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Last Update: June 26, 2023.

Continuing Education Activity

Adapalene is a topical retinoid with FDA approval for treating acne vulgaris. Retinoids are vitamin A derivatives that are typically described in terms of generations with increased specificity of retinoic acid receptor (RAR) affinity with later generations. Clinicians use retinoids are used to treat a wide variety of skin disorders. Adapalene also has multiple off-label therapeutic applications, including the treatment of verrucae, molluscum contagiosum, Darier disease, Fox-Fordyce disease, Dowling-Degos disease, photoaging, pigmentary disorders, actinic keratoses, and alopecia areata. This activity outlines the indications, contraindications, interactions, monitoring, and other therapeutic information pertinent to members of an interprofessional team in the care of patients on adapalene therapy.


  • Identify the approved indications for adapalene.
  • Describe the mechanism of action of adapalene.
  • Summarize the adverse effect profile of adapalene.
  • Review interprofessional team strategies for improving care coordination and communication to improve patient outcomes using adapalene.
Access free multiple choice questions on this topic.


Adapalene is a topical retinoid that is FDA-approved for treating acne vulgaris.[1][2] Like other retinoids, adapalene has been used off-label for various skin conditions, including verrucae, molluscum contagiosum, Darier disease, Fox-Fordyce disease, Dowling-Degos disease, photoaging, pigmentary disorders such as melasma and post-inflammatory hyperpigmentation, actinic keratoses, and alopecia areata.[3] Additionally, adapalene and adapalene analogs are investigated for potential anti-microbial, anti-cancer, and neuroprotective effects.[4]

Adapalene was initially FDA-approved in 1996 for acne in patients 12 years of age or older. The FDA-approved adapalene 0.1% gel as an over-the-counter acne treatment in patients 12 and older in 2016. Formulations of adapalene 0.1% lotion, cream, and 0.3% gel are available by prescription only.

Retinoids are vitamin A derivatives that are typically described in terms of generations with increased specificity of retinoic acid receptor (RAR) affinity with later generations. Adapalene is a third-generation synthetic retinoid developed to improve the side effect profile compared to tretinoin. This first-generation topical retinoid more closely resembles natural vitamin A in structure.[4] Second-generation retinoids are oral medications. The primary representative of the second generation is acitretin, which has enhanced benefits to the skin but has limited therapeutic use due to the significant risk of toxicity and is contraindicated for people of childbearing potential.[5]

Third-generation retinoids include adapalene, tazarotene, and bexarotene. Of the third generation, bexarotene is a synthetic retinoid that binds exclusively to retinoid X receptors (RXR). Adapalene and tazarotene have higher specificity for RAR-gamma and RAR-beta and do not interact with RXRs making them suitable for topical administration with minimal systemic absorption.[6] Trifarotene is a fourth-generation topical retinoid FDA-approved in 2019 for treating acne with a 20-fold greater affinity for RAR-gamma, the most dominant subtype in the skin, and has no affinity for RXR receptors.[7]

Retinoids modulate epidermal growth and differentiation, stimulate humoral and cellular immunity, decrease the inflammatory response, and reduce cell proliferation. The diverse biological actions of retinoids make them ideal for treating various skin disorders.[5] Topical retinoids are recommended as first-line therapy to treat acne vulgaris, alone or in combination with other acne medications.[8] Topical retinoids used in treating acne vulgaris include adapalene, tretinoin, tazarotene, and trifarotene. Topical retinoids target two pathogenic mechanisms of acne vulgaris: microcomedone formation, which is the precursor of all forms of acne lesions, and the inflammatory response.[6]

Conventional teaching indicates that the retinoids used to treat acne have varying grades of efficacy and tolerability. Adapalene is perceived to be the least effective but the best tolerated. Tretinoin is understood to have moderate efficacy and tolerability. Tazarotene has maximum efficacy but is not tolerated due to skin irritation. Currently, conventional teaching does not yet compare trifarotene with prior generations; however, it has increased the ability to induce gene expression compared to tazarotene.[7]

Despite these conventions, studies support that adapalene is more efficacious in treating acne vulgaris than other retinoids. A meta-analysis including five randomized controlled trials suggested that adapalene 0.1% gel had similar efficacy but enhanced tolerability in acne treatment compared to tretinoin 0.025% gel. Adapalene has also been compared to tretinoin in a vehicle formulation of microsphere gel, which allows for tretinoin to be delivered primarily to the epidermis to decrease irritation and increase tolerability. A randomized controlled trial of tolerability, safety, and efficacy of adapalene gel 0.1% and tretinoin 0.1% microsphere gel revealed that the efficacy was comparable in total, non-inflammatory, and inflammatory lesions. However, the adapalene patient group exhibited significantly enhanced cutaneous tolerability.[9]

Adapalene also performs well when compared to tazarotene. In a 12-week randomized, evaluator-blinded study comparing adapalene 0.3% gel and tazarotene 0.1% gel, each group had a clinically significant reduction in total lesion counts. A 61% reduction in acne lesions occurred with the administration of adapalene, with a 57% reduction in the tazarotene group. Adapalene, 0.3% gel, had equivalent efficacy to tazarotene 0.1% gel. However, patients using adapalene experienced less irritation than patients in the tazarotene-treated group.[10]

Adapalene has additional advantages when compared to other retinoids. Adapalene is a more stable molecule, which leads to less concern for molecular photodegradation, allowing for use during daylight hours. This stability contrasts with both tretinoin and tazarotene, which are photolabile. The stability of adapalene allows for use in combination with benzoyl peroxide, which has a synergist effect. A randomized double-blinded study of topical adapalene 0.3%-benzoyl peroxide 2.5% demonstrated significantly greater efficacy in patients with moderate-to-severe inflammatory, non-nodulocystic acne. With the synergistic effect of benzoyl peroxide, adapalene 0.3% increases patient treatment options for moderate to severe acne.[2][11]

Mechanism of Action

Adapalene is a third-generation topical retinoid prescribed for the treatment of acne vulgaris.[12] Adapalene is a naphthoic acid derivative designed to be more structurally rigid than previous retinoid generations, which decreases its ability to bind multiple retinoid receptors, thus reducing off-target effects. Adapalene is an active metabolite and therefore requires no metabolic conversion. The adamantane nucleus is the chemical moiety that allows adapalene to attach to RAR-beta and RAR-gamma. This complex binds DNA through retinoic acid response elements and induces gene transcription, leading to downstream keratinocyte proliferation and differentiation. As a result, adapalene decreases microcomedone formations, exfoliates mature comedones, and has anti-inflammatory effects.[4][9] Of note, the adamantane nucleus is a component found in multiple other drugs, including antivirals and anti-hypoglycemic agents. Adapalene and newer analogs are under investigation for new potential therapeutic uses due to the antiproliferative, antibacterial, and neuroprotective activity attributed to the adamantane moiety.[13][4]

The pathogenesis of acne vulgaris is multifactorial. However, the main factors associated with acneiform lesion development are follicular hyperkeratinization, sebum production by sebaceous glands, and inflammation. In acne-prone patients, keratinocytes accumulate in the lumen of the hair follicle due to increased keratinocyte proliferation and cohesiveness, leading to the formation of a keratotic plug, resulting in the microcomedone. The microcomedone is the precursor to all visible acne lesions like open comedones, closed comedones, inflammatory papules, pustules, and nodulocystic lesions. Adapalene normalizes the differentiation of follicular epithelial cells to prevent microcomedone formation. In addition, adapalene, when applied topically, penetrates the hair follicles due to its lipophilic nature.

In addition to follicular hyperkeratinization, acne is also a disorder associated with inflammation. Propionibacterium acnes is a gram-positive, anaerobic rod found in the sebaceous follicle. P. acnes is present in both acne-prone individuals and those without acne. The hypothesis is that there may be differences in the strains of P. acnes or in the host response to P. acnes, which leads to its varying degrees of pathogenicity. P. acnes release mediators that contribute to comedones rupture and stimulate inflammatory cells. P. acnes stimulates the toll-like receptor II (TLR-2) pathway, which releases pro-inflammatory modulators. This action leads to neutrophil recruitment and the release of enzymes that result in follicular epithelium rupture. One mediator, IL-12, promotes a TH1 immune response. Adapalene is thought to suppress polymorphonuclear lymphocyte chemotaxis and down-regulate 15-lipoxygenase and TLR-2, contributing to its anti-inflammatory effects. The anti-inflammatory action of adapalene is comparable to betamethasone-17-valerate and indomethacin.[9][6]


Absorption: Systemic exposure of adapalene following topical application of adapalene gel is minimal. 

Distribution: Adapalene drug molecules are distributed in the epidermis and dermis.[14]

Metabolism: Information regarding adapalene metabolism in humans is unavailable, although it is known to accumulate in the liver. The major products of metabolism are glucuronides. Approximately 25% of the adapalene is metabolized, and the rest is excreted in unchanged form.

Excretion: The terminal apparent half-life is 7 to 51 hours. Excretion of adapalene is primarily through the biliary route.


Adapalene is applied to a clean face once daily in the morning or at bedtime. The patient should wash the face with a gentle cleanser and allow the face to dry thoroughly. Then a pea-sized amount of adapalene should be applied as a thin layer to the entire face. Avoiding application to eyelids, lips, and mucous membranes is necessary. Patients can apply an oil-free moisturizer over adapalene to help decrease the risk of irritation. As there is a risk of photosensitivity with topical retinoids, the clinician should also recommend an oil-free sunscreen and warn the patient against excessive sun exposure.

One reason for treatment failure with topical retinoids is the initial skin irritation that occurs and maximizes in intensity within two weeks of treatment. This initial mild irritation can lead to the discontinuation of therapy.[15] There are several options for treatment regimens to decrease the initial irritation as the skin acclimates to daily use. Options include application every other day, short contact therapy, or choosing a different drug vehicle.[6]

An investigation in modulating treatment regimens with adapalene 0.1%-benzoyl peroxide 2.5% combination in the first four weeks demonstrated no difference in efficacy outcomes at 12 weeks. The treatment regimens investigated were topical nightly application, limited exposure application of 3 hours, every other night application, and nightly application with a gentle moisturizer.[11]

Use in Specific Patient Populations

Patients with Renal Impairment: No information regarding the use of adapalene in patients with renal impairment is provided in product labeling. 

Patients with Hepatic Impairment: No information regarding the use of adapalene in patients with hepatic impairment is provided in product labeling.

Pregnancy Considerations: Adapalene was pregnancy category C under the prior FDA pregnancy classification system and should be avoided in pregnant patients. . Oral exposure of pregnant animals to high doses of third-generation retinoids resulted in retinoid embryopathies. Topical administration of adapalene results in minimal systemic absorption, with less than 0.01% absorbed systemically and clearance from plasma within 72 hours of application. The most sensitive adverse effect of retinoids is possible teratogenicity. Vitamin A is essential for embryo-fetal development. Both deficiencies and overabundance can disrupt normal development. First and second-generation retinoids are known to cause retinoid embryopathies with oral administration. Topically applied retinoids, including first-generation tretinoin, have minimal systemic absorption, and third- and fourth-generation retinoids are designed to minimize off-target effects. Concern for teratogenicity was first raised because three reports to the FDA from 1986 to 1989 highlight holoprosencephaly in infants exposed to topical retinoids in utero. Subsequent case series and observational cohorts did not corroborate the initial reports.[7] 

A recent systematic literature review and meta-analysis evaluating first-trimester exposure to topical retinoids demonstrated no clear increase in the risk of retinoid embryopathy. However, the lack of epidemiologic data is reason enough to approach the use of topical retinoids during pregnancy with caution. Topical retinoids are not currently recommended during pregnancy. Therefore, adapalene should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.[5][16] 

Breastfeeding Considerations:  The use of topical adapalene has not been evaluated during breastfeeding. Adapalene is probably a low risk to the nursing infant because it is poorly absorbed after topical application, and blood levels are minimal with prolonged therapy. However, clinicians should advise breastfeeding mothers that adapalene should not be applied to the nipple area and ensure that the infant's skin does not come into direct contact with skin areas treated with adapalene. Clinicians should generally avoid prescribing during breastfeeding due to potential risks to the infant.[17]

Adverse Effects

Adverse reactions reported from adapalene include photosensitivity, irritation, redness, dryness, itching, and burning. These are usually mild adverse events.[8][18]

Adapalene is less irritating compared to other topical retinoids. In a blinded, randomized, controlled, parallel-group study of 591 acne patients, a combined safety analysis conducted in the United States and Europe compared adapalene 0.1% gel and tretinoin 0.025% gel. The number of patients discontinuing the study due to adverse events was about twice as high in those using tretinoin (2.4%) compared to adapalene (1.3%). There were no systemic adverse reactions noted in the study. Most of the adverse reactions observed were related to skin irritation. Multiple other studies have demonstrated similar findings.[9][6] 

Adapalene 0.1% and 0.3% have also been compared to tazarotene in multiple studies showing adapalene to be non-inferior in efficacy and demonstrated superior tolerability.[10][19] The enhanced tolerability of adapalene has been attributed, in part, to the selective affinity to the nuclear RAR-beta and RAR-gamma receptors, as opposed to RAR-alpha. The decreased risk of skin irritation may contribute to better long-term compliance. Exposure to ultraviolet light should be minimized in patients using adapalene gel. Patients exposed to high levels of sun exposure and sensitive to sunlight should exercise caution. Using sunscreen and protective clothing over adapalene-treated areas is suggested when patients cannot avoid exposure to the sunlight.[4]

Rare, severe allergic reactions characteristically demonstrate pruritus, facial edema, lip swelling, and eyelid swelling.[15][20] If a patient experiences anaphylactic reactions with symptoms, including facial swelling, hives, chest pain, or shortness of breath, adapalene should be discontinued, and the patient should seek immediate medical evaluation.


Contraindications include a history of hypersensitivity to adapalene or any excipients used in the product or other retinoids. According to product labeling, relative contraindications include pregnancy, photosensitive disorder, eczema, sunburn, or concomitant use of other potentially irritating skincare products.


The patient should have a reassessment for efficacy in 12 weeks or sooner if severe adverse effects occur. According to the American Academy of Dermatology, laboratory evaluation is recommended for patients with acne and additional signs of androgen excess.[21]


If the adapalene is applied excessively, marked redness, scaling, or skin discomfort may occur. In addition, according to product labeling, chronic ingestion of the drug may lead to the same adverse drug reactions associated with excessive oral intake of vitamin A. 

Enhancing Healthcare Team Outcomes

Adapalene is a topical retinoid that is FDA-approved for the treatment of acne vulgaris and used off-label in the treatment of many conditions, including verrucae, molluscum contagiosum, Darier disease, Fox-Fordyce disease, Dowling-Degos disease, photoaging, pigmentary disorders such as melasma and post-inflammatory hyperpigmentation, actinic keratoses, and alopecia areata. The multidimensional acne global grading system, which incorporates primary acne lesions (comedones, papules, and nodules) and associated secondary changes (postinflammatory hyperpigmentation and scarring), is useful in the comprehensive clinical evaluation of acne to guide appropriate treatment choices.[22]

Clinicians and specialists who prescribe this agent and pharmacists interacting with patients must be fully aware of its side effects and contraindications. Pharmacists will also perform thorough medication reconciliation. Due to the lack of epidemiologic data, clinicians should not prescribe adapalene to women during pregnancy or breastfeeding.[9][16] Dermatology specialty-trained nursing staff should be on hand to counsel and follow up with patients on adapalene therapy. Nursing should assess patient compliance, answer questions regarding dosing/administration, monitor for adverse events, and promptly alert the prescriber if present. ALl interprofessional team members must maintain meticulous documentation in the patient's medical record and communicate with other team members as necessary so therapeutic modifications can be implemented if appropriate. Collaboration between all these disciplines in an interprofessional team can optimize adapalene therapy while minimizing adverse effects. [Level 5]

Review Questions


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Tan J, Bissonnette R, Gratton D, Kerrouche N, Canosa JM. The safety and efficacy of four different fixed combination regimens of adapalene 0.1%/benzoyl peroxide 2.5% gel for the treatment of acne vulgaris: results from a randomised controlled study. Eur J Dermatol. 2018 Aug 01;28(4):502-508. [PubMed: 30187864]
Bagatin E, Gonçalves HS, Sato M, Almeida LMC, Miot HA. Comparable efficacy of adapalene 0.3% gel and tretinoin 0.05% cream as treatment for cutaneous photoaging. Eur J Dermatol. 2018 Jun 01;28(3):343-350. [PubMed: 30105991]
Rusu A, Tanase C, Pascu GA, Todoran N. Recent Advances Regarding the Therapeutic Potential of Adapalene. Pharmaceuticals (Basel). 2020 Aug 28;13(9) [PMC free article: PMC7558148] [PubMed: 32872149]
Williams AL, Pace ND, DeSesso JM. Teratogen update: Topical use and third-generation retinoids. Birth Defects Res. 2020 Sep;112(15):1105-1114. [PubMed: 32643315]
Chivot M. Retinoid therapy for acne. A comparative review. Am J Clin Dermatol. 2005;6(1):13-9. [PubMed: 15675886]
Kassir M, Karagaiah P, Sonthalia S, Katsambas A, Galadari H, Gupta M, Lotti T, Wollina U, Abdelmaksoud A, Grabbe S, Goldust M. Selective RAR agonists for acne vulgaris: A narrative review. J Cosmet Dermatol. 2020 Jun;19(6):1278-1283. [PubMed: 32100454]
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Sardana K, Sehgal VN. Retinoids: fascinating up-and-coming scenario. J Dermatol. 2003 May;30(5):355-80. [PubMed: 12773802]
Thiboutot D, Arsonnaud S, Soto P. Efficacy and tolerability of adapalene 0.3% gel compared to tazarotene 0.1% gel in the treatment of acne vulgaris. J Drugs Dermatol. 2008 Jun;7(6 Suppl):s3-10. [PubMed: 18575220]
Stein Gold L, Weiss J, Rueda MJ, Liu H, Tanghetti E. Moderate and Severe Inflammatory Acne Vulgaris Effectively Treated with Single-Agent Therapy by a New Fixed-Dose Combination Adapalene 0.3 %/Benzoyl Peroxide 2.5 % Gel: A Randomized, Double-Blind, Parallel-Group, Controlled Study. Am J Clin Dermatol. 2016 Jun;17(3):293-303. [PMC free article: PMC4863916] [PubMed: 26945741]
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Najafi-Taher R, Ghaemi B, Amani A. Delivery of adapalene using a novel topical gel based on tea tree oil nano-emulsion: Permeation, antibacterial and safety assessments. Eur J Pharm Sci. 2018 Jul 30;120:142-151. [PubMed: 29684425]
Cunliffe WJ, Caputo R, Dreno B, Förström L, Heenen M, Orfanos CE, Privat Y, Robledo Aguilar A, Meynadier J, Alirezai M, Jablonska S, Shalita A, Weiss JS, Chalker DK, Ellis CN, Greenspan A, Katz HI, Kantor I, Millikan LE, Swinehart JM, Swinyer L, Whitmore C, Czernielewski J, Verschoore M. Clinical efficacy and safety comparison of adapalene gel and tretinoin gel in the treatment of acne vulgaris: Europe and U.S. multicenter trials. J Am Acad Dermatol. 1997 Jun;36(6 Pt 2):S126-34. [PubMed: 9204091]
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Zaenglein AL, Pathy AL, Schlosser BJ, Alikhan A, Baldwin HE, Berson DS, Bowe WP, Graber EM, Harper JC, Kang S, Keri JE, Leyden JJ, Reynolds RV, Silverberg NB, Stein Gold LF, Tollefson MM, Weiss JS, Dolan NC, Sagan AA, Stern M, Boyer KM, Bhushan R. Guidelines of care for the management of acne vulgaris. J Am Acad Dermatol. 2016 May;74(5):945-73.e33. [PubMed: 26897386]
Bernardis E, Shou H, Barbieri JS, McMahon PJ, Perman MJ, Rola LA, Streicher JL, Treat JR, Castelo-Soccio L, Yan AC. Development and Initial Validation of a Multidimensional Acne Global Grading System Integrating Primary Lesions and Secondary Changes. JAMA Dermatol. 2020 Mar 01;156(3):296-302. [PMC free article: PMC6990806] [PubMed: 31995147]

Disclosure: Leila Tolaymat declares no relevant financial relationships with ineligible companies.

Disclosure: Heidi Dearborn declares no relevant financial relationships with ineligible companies.

Disclosure: Patrick Zito declares no relevant financial relationships with ineligible companies.

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Bookshelf ID: NBK482509PMID: 29494115


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