NDC 71589-008 Adapalene


NDC Product Code 71589-008

NDC 71589-008-15

Package Description: 1 TUBE in 1 CARTON > 15 g in 1 TUBE

NDC 71589-008-45

Package Description: 1 TUBE in 1 CARTON > 45 g in 1 TUBE

NDC 71589-008-46

Package Description: 1 BOTTLE, PUMP in 1 CARTON > 45 g in 1 BOTTLE, PUMP

NDC Product Information

Adapalene with NDC 71589-008 is a a human prescription drug product labeled by Aleor Dermaceuticals Limited. The generic name of Adapalene is adapalene. The product's dosage form is gel and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 722111.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

Product Type: Human Prescription Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Adapalene Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • POLOXAMER 124 (UNII: 1S66E28KXA)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Retinoid - [EPC] (Established Pharmacologic Class)
  • Retinoids - [CS]

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Aleor Dermaceuticals Limited
Labeler Code: 71589
FDA Application Number: ANDA213508 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: ANDA - A product marketed under an approved Abbreviated New Drug Application. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 06-26-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Adapalene Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

1 Indications And Usage

Adapalene gel, 0.3% is indicated for the topical treatment of acne vulgaris in patients 12 years of age and older.

2 Dosage And Administration

Apply a thin film of adapalene gel, 0.3% to the entire face and any other affected areas of the skin once daily in the evening, after washing gently with a non-medicated soap. Avoid application to the areas of skin around eyes, lips, and mucous membranes. A mild transitory sensation of warmth or slight stinging may occur shortly after the application of adapalene gel, 0.3%.  Patients should be instructed to minimize sun exposure. Patients may be instructed to use moisturizers for relief of dry skin or irritation.If therapeutic results are not noticed after 12 weeks of treatment, therapy should be re-evaluated.For topical use only. Not for ophthalmic, oral or intravaginal use.

3 Dosage Forms And Strengths

Each gram of adapalene gel USP, 0.3% contains 3 mg adapalene, USP in an off-white aqueous gel.

4 Contraindications

Adapalene gel, 0.3% should not be administered to individuals who are hypersensitive to adapalene or any of the components in the gel vehicle.

5.1 Ultraviolet Light And Environmental Exposure

Exposure to sunlight, including sunlamps, should be minimized during use of adapalene gel, 0.3%. Patients who normally experience high levels of sun exposure, and those with inherent sensitivity to sun, should be warned to exercise caution. Use of sunscreen products and protective clothing over treated areas is recommended when exposure cannot be avoided. Weather extremes, such as wind or cold, also may be irritating to patients under treatment with adapalene gel, 0.3%.

5.2 Local Cutaneous Reactions

Certain cutaneous signs and symptoms of treatment such as erythema, scaling, dryness, and stinging/burning were reported with use of adapalene gel, 0.3%. These were most likely to occur during the first four weeks of treatment, were mostly mild to moderate in intensity, and usually lessened with continued use of the medication. Depending upon the severity of these side effects, patients should be instructed to either use a moisturizer, reduce the frequency of application of adapalene gel, 0.3% or discontinue use.Avoid contact with the eyes, lips, angles of the nose, and mucous membranes. The product should not be applied to cuts, abrasions, eczematous or sunburned skin. As with other retinoids, use of "waxing" as a depilatory method should be avoided on skin treated with adapalene.As adapalene gel has the potential to induce local irritation in some patients, concomitant use of other potentially irritating topical products (medicated or abrasive soaps and cleansers, soaps and cosmetics that have a strong drying effect and products with high concentrations of alcohol, astringents, spices, or lime) should be approached with caution.

5.3 Allergic/ Hypersensitivity Reactions

Reactions characterized by symptoms such as pruritus, face edema, eyelid edema, and lip swelling, requiring medical treatment have been reported during postmarketing use of adapalene. A patient should stop using adapalene gel, 0.3% and consult a doctor if experiencing allergic or anaphylactoid/anaphylactic reactions (e.g., skin rash, pruritus, hives, chest pain, edema, and shortness of breath) during treatment.

6.1 Clinical Trials Experience

Because clinical trials are conducted under widely varying conditions, adverse reactions rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.In the multi-center, controlled clinical trial, signs and symptoms of local cutaneous irritation were monitored in 258 acne patients who used adapalene gel, 0.3% once daily for 12 weeks. Of the patients who experienced cutaneous irritation (erythema, scaling, dryness, and/or burning/stinging), the majority of cases were mild to moderate in severity, occurred early in treatment and decreased thereafter.  The incidence of local cutaneous irritation with adapalene gel, 0.3% from the controlled clinical study is provided in the following table: Table 1: Physician assessed local cutaneous irritation with Adapalene Gel * Total number of subjects with local cutaneous data for at least one post-Baseline evaluation. Incidence of Local Cutaneous Irritation with Adapalene Gel, 0.3% from Controlled Clinical Study (N = 253*) Maximum Severity Scores Higher Than Baseline Mild Moderate Severe Erythema 66 (26.1%) 33 (13.0%) 1 (0.4%) Scaling 110 (43.5%) 47 (18.6%) 3 (1.2%) Dryness 113 (44.7%) 43 (17.0%) 2 (0.8%) Burning/Stinging 72 (28.5%) 36 (14.2%) 9 (3.6%) Table 2: Patient reported local cutaneous adverse reactions with Adapalene Gel *Selected adverse reactions defined by investigator as Possibly, Probably or Definitely Related Adapalene Gel, 0.3% Vehicle Gel N=258 N=134 Related* Adverse Reactions 57 (22.1%) 6 (4.5%)                Dry Skin 36 (14%) 2 (1.5%)                Skin Discomfort 15 (5.8%) 0 (0.0%)                Desquamation 4 (1.6%) 0 (0.0%)Related adverse reactions from the controlled clinical trial that occurred in greater than 1% of patients who used adapalene gel, 0.3% once daily included: dry skin (14.0%), skin discomfort (5.8%), pruritus (1.9%), desquamation (1.6%), and sunburn (1.2%). The following selected adverse reactions occurred in less than 1% of patients: acne flare, contact dermatitis, eyelid edema, conjunctivitis, erythema, pruritus, skin discoloration, rash, and eczema.In a one-year, open-label safety study of 551 patients with acne who received adapalene gel, 0.3%, the pattern of adverse reactions was similar to the 12-week controlled study.

6.2 Postmarketing Experience

The following adverse reactions have been identified during post approval use of adapalene: skin irritation, application site pain, face edema, eyelid edema, lip swelling, and angioedema. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate the frequency or establish a causal relationship to drug exposure.

7.1 Concomitant Topical Medications

As adapalene gel, 0.3% has the potential to induce local irritation in some patients, concomitant use of other potentially irritating topical products (medicated or abrasive soaps and cleansers, soaps and cosmetics that have a strong drying effect, and products with high concentrations of alcohol, astringents, spices, or lime) should be approached with caution. Particular caution should be exercised in using preparations containing sulfur, resorcinol, or salicylic acid in combination with adapalene gel, 0.3%. If these preparations have been used, it is advisable not to start therapy with adapalene gel, 0.3%, until the effects of such preparations have subsided.No formal drug-drug interaction studies were conducted with adapalene gel, 0.3%.

8.1 Pregnancy

  • Teratogenic effects. Pregnancy Category C.Retinoids may cause fetal harm, when administered to pregnant women. Adapalene has been shown to be teratogenic in rats and rabbits when administered orally (see Animal Data below). There are no adequate and well-controlled studies in pregnant women. Adapalene gel, 0.3% should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. The safety and efficacy of adapalene gel, 0.3% in pregnancy has not been established.Human DataIn clinical trials involving adapalene gel, 0.3% in the treatment of acne vulgaris, women of child-bearing potential initiated treatment only after having had a negative pregnancy test and used effective birth control measures during therapy. However, 6 women treated with adapalene gel, 0.3% became pregnant. One patient elected to terminate the pregnancy, two patients delivered healthy babies by normal delivery, two patients delivered prematurely and the babies remained in intensive care until reaching a healthy state and one patient was lost to follow-up.Animal DataNo teratogenic effects were seen in rats at oral doses of 0.15 to 5.0 mg/kg/day adapalene representing up to 6 times the maximum recommended human dose (MRHD) based on mg/m  comparisons. Adapalene has been shown to be teratogenic in rats and rabbits when administered orally at doses ≥ 25 mg/kg representing 32 and 65 times, respectively, the MRHD based on mg/m  comparisons. Findings included cleft palate, microphthalmia, encephalocele and skeletal abnormalities in the rat and umbilical hernia, exophthalmos and kidney and skeletal abnormalities in the rabbit.Cutaneous teratology studies in rats and rabbits at doses of 0.6, 2.0, and 6.0 mg/kg/day exhibited no fetotoxicity and only minimal increases in supernumerary ribs in both species and delayed ossification in rabbits. Systemic exposure (AUC0 to 24h) to adapalene 0.3% gel at topical doses of 6.0 mg/kg/day in rats and rabbits represented 5.7 and 28.7 times, respectively, the exposure in acne patients treated with adapalene 0.3% gel applied to the face, chest and back (2 grams applied to 1000 cm2of acne involved skin).

8.3 Nursing Mothers

It is not known whether adapalene is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when adapalene gel, 0.3% is administered to a nursing woman.

8.4 Pediatric Use

Safety and effectiveness have not been established in pediatric patients below the age of 12.

8.5 Geriatric Use

Clinical studies of adapalene gel, 0.3% did not include subjects 65 years of age and older to determine whether they respond differently than younger subjects. Safety and effectiveness in geriatric patients age 65 and above have not been established.

10 Overdosage

Adapalene gel, 0.3% is intended for topical use only. If the medication is applied excessively, no more rapid or better results will be obtained and marked redness, scaling, or skin discomfort may occur.  Chronic ingestion of the drug may lead to the same side effects as those associated with excessive oral intake of vitamin A.

11 Description

Adapalene Gel USP, 0.3% contains adapalene USP, 0.3% (3 mg/g) in a topical aqueous gel for use in the treatment of acne vulgaris, consisting of carbopol 980, edetate disodium, methylparaben, poloxamer 124, propylene glycol, purified water, and sodium hydroxide. May contain hydrochloric acid for pH adjustment.The chemical name of adapalene, USP is 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthoic acid. It is a white to off-white powder, which is soluble in tetrahydrofuran, very slightly soluble in ethanol, and practically insoluble in water. The molecular formula is C28H28O3 and molecular weight is 412.53. Adapalene, USP is represented by the following structural formula.

12.1 Mechanism Of Action

Adapalene binds to specific retinoic acid nuclear receptors but does not bind to cytosolic receptor protein.  Biochemical and pharmacological profile studies have demonstrated that adapalene is a modulator of cellular differentiation, keratinization, and inflammatory processes. However, the significance of these findings with regard to the mechanism of action of adapalene for the treatment of acne is unknown.

12.2 Pharmacodynamics

Clinical pharmacodynamic studies have not been conducted for adapalene gel, 0.3%.

12.3 Pharmacokinetics

Systemic exposure of adapalene following topical application of adapalene gel was evaluated in a clinical study. Sixteen acne patients were treated once daily for 10 days with 2 grams of adapalene gel, 0.3% applied to the face, chest and back, corresponding to approximately 2 mg/cm2. Fifteen patients had quantifiable (LOQ = 0.1 ng/mL) adapalene levels resulting in a mean Cmax of 0.553 ± 0.466 ng/mL on Day 10 of treatment. The mean AUC0 to 24hr was 8.37 ± 8.46 ng.h/mL as determined in 15 of the 16 patients on Day 10. The terminal apparent half-life, determined in 15 of 16 patients, ranged from 7 to 51 hours, with a mean of 17.2 ± 10.2 hours. Adapalene was rapidly cleared from plasma and was not detected 72 hours after the last application for all but one subject. Exposure of potential circulating metabolites of adapalene was not measured. Excretion of adapalene appears to be primarily by the biliary route.In another clinical study in patients with moderate to moderately severe acne, adapalene gel, 0.3% or adapalene gel, 0.1% was applied to the face and optionally to the trunk, once daily for 12 weeks. Seventy-eight (78) patients had plasma adapalene levels evaluated at Weeks 2, 8, and 12.  Of the 209 plasma samples analyzed, adapalene concentrations were below the limit of detection (LOD = 0.15 ng/mL) of the method in all samples but three. For the three samples, traces of adapalene below the limit of quantification (LOQ = 0.25 ng/mL) of the method were found. One of these samples was taken at Week 12 from a male patient treated with adapalene gel, 0.3% who treated the face and the trunk for eight weeks (thereafter, only the face was treated). The second and third samples were from the Week 2 and 12 visits of a female patient treated with adapalene gel, 0.1% who treated only the face for 12 weeks. In this study, the average daily usage of product was 1 g/day.

13.1 Carcinogenesis, Mutagenesis, Impairment Of Fertility

Carcinogenicity studies with adapalene have been conducted in mice at topical doses of 0.4, 1.3, and 4.0 mg/kg/day, and in rats at oral doses of 0.15, 0.5, and 1.5 mg/kg/day. These doses are up to 3 times (mice) and 2 times (rats) in terms of mg/m /day the potential exposure at the maximum recommended human dose (MRHD), assumed to be 2.5 grams adapalene gel, 0.3%. In the oral study, increased incidence of benign and malignant pheochromocytomas in the adrenal medullas of male rats was observed.No photocarcinogenicity studies were conducted. Animal studies have shown an increased risk of skin neoplasms with the use of pharmacologically similar drugs (e.g., retinoids) when exposed to UV irradiation in the laboratory or to sunlight. Although the significance of these studies to human use is not clear, patients should be advised to avoid or minimize exposure to either sunlight or artificial UV irradiation sources.Adapalene did not exhibit mutagenic or genotoxic effects in vitro (Ames test, Chinese hamster ovary cell assay, mouse lymphoma TK assay) and in vivo (mouse micronucleus test).Reproductive function and fertility studies were conducted in rats administered oral doses of adapalene in amounts up to 20 mg/kg/day (up to 26 times the MRHD based on mg/m  comparisons). No effects of adapalene were found on the reproductive performance or fertility of the F0 males or females. There were also no detectable effects on the growth, development and subsequent reproductive function of the F1 offspring.

14 Clinical Studies

The safety and efficacy of once daily use of adapalene gel, 0.3% for treatment of acne vulgaris were assessed in one 12 week, multi-center, controlled, clinical study, conducted in a total of 653 patients 12 to 52 years of age with acne vulgaris of mild to moderate severity. All female patients of child-bearing potential enrolled in the study were required to have a negative urine pregnancy test at the beginning of the study and were required to practice a highly effective method of contraception during the study. Female patients who were pregnant, nursing or planning to become pregnant were excluded from the study.Patients enrolled in the study were Caucasian (72%), Hispanic (12%), African-American (10%), Asian (3%), and other (2%). An equal number of males (49.5%) and females (50.5%) enrolled. Success was defined as "Clear" or "Almost Clear" in the Investigator's Global Assessment (IGA). The success rate, mean reduction, and percent reduction in acne lesion counts from Baseline after 12 weeks of treatment are presented in the following table: Table 3: Clinical study primary efficacy results at Week 12 Adapalene Gel, 0.3% Adapalene Gel, 0.1% Vehicle Gel N=258 N=261 N=134 IGA Success Rate 53 (21%) 41 (16%) 12 (9%) Inflammatory Lesions Mean Baseline Count Mean Absolute (%) Reduction 27.7 14.4 (51.6%) 28.1 13.9 (49.7%) 27.2 11.2 (40.7%) Non-inflammatory Lesions Mean Baseline Count Mean Absolute (%) Reduction 39.4 16.3 (39.7%) 41.0 15.2 (35.2%) 40.0 10.3 (27.2%) Total Lesions Mean Baseline Count Mean Absolute (%) Reduction 67.1 30.6 (45.3%) 69.1 29.0 (41.8%) 67.2 21.4 (33.7%)

16 How Supplied/Storage And Handling

Adapalene gel USP, 0.3% is supplied in the following size.15 g tube – NDC 71589-008-1545 g tube – NDC 71589-008-4545 g pump – NDC 71589-008-46Storage: Store at controlled room temperature 68° to 77°F (20° to 25°C) with excursions permitted between 59° to 86°F (15° to 30°C). Protect from freezing. Keep out of reach of children.

17 Patient Counseling Information

  • "See FDA-approved patient labeling (Patient Information)"Information for PatientsPatients using adapalene gel, 0.3%, should receive the following information and instructions:This medication is to be used only as directed by the physician.Do not use more than the recommended amount and do not apply more than once daily as this will not produce faster results, but may increase irritation.Apply a thin film of adapalene gel, 0.3% to the entire face and any other affected areas of the skin once daily in the evening, after washing gently with a non-medicated soap.Avoid contact with the eyes, lips, angles of the nose, and mucous membranes.Moisturizers may be used if necessary; however, products containing alpha hydroxy or glycolic acids should be avoided.Exposure of the eye to this medication may result in reactions such as swelling, conjunctivitis, and eye irritation.This medication should not be applied to cuts, abrasions, eczematous, or sunburned skin.Wax depilation should not be performed on treated skin due to the potential for skin erosions.Minimize exposure to sunlight including sunlamps. Recommend the use of sunscreen products and protective apparel (e.g., hat) when exposure cannot be avoided.During the early weeks of therapy, an apparent exacerbation of acne may occur. This may be due to the action of the medication on previously unseen lesions and should not be considered a reason to discontinue therapy.Contact the doctor if skin rash, pruritus, hives, chest pain, edema, and shortness of breath occurs, as these may be signs of allergy or hypersensitivity.It is for external use only.Manufactured by:Aleor Dermaceuticals Ltd.,Karakhadi, Vadodara 391450, India.Mfg. Lic. No.: G/25/2216Manufactured for:Aleor Dermaceuticals Ltd.,Karakhadi, Vadodara 391450, India.Revised: 6/2020Patient InformationAdapalene (a dap' a leen) Gel, 0.3% Important: For use on the skin only (topical). Do not use adapalene gel, 0.3% in or on your mouth, eyes, or vagina.Read this Patient Information that comes with adapalene gel, 0.3% before you start using it and each time you get a refill. There may be new information. This leaflet does not take the place of talking with your doctor about your treatment or your medical condition. If you have any questions about adapalene gel, 0.3%, talk with your doctor or pharmacist.What is adapalene gel, 0.3%?Adapalene gel, 0.3% is a prescription medicine for skin use only (topical) used to treat acne vulgaris in people 12 years of age and older. Acne vulgaris is a condition in which the skin has blackheads, whiteheads and pimples.It is not known if adapalene gel, 0.3% is safe and effective in children younger than 12 years of age or in people 65 years of age and older.Who should not use adapalene gel, 0.3%?Do not use adapalene gel, 0.3% if you:  are allergic to adapalene or any of the ingredients in adapalene gel, 0.3%. See the end of this Patient Information for a complete list of ingredients in adapalene gel.What should I tell my doctor before using adapalene gel, 0.3%?Before you use adapalene gel, 0.3%, tell your doctor if you:have other skin problems, including cuts or sunburnhave any other medical conditionsare pregnant or planning to become pregnant. It is not known if adapalene gel, 0.3% can harm your unborn baby. Talk to your doctor if you are pregnant or plan to become pregnant.are breastfeeding or plan to breastfeed. It is not known if adapalene gel, 0.3% passes into your breast milk and if it can harm your baby. Talk to your doctor about the best way to feed your baby if you use adapalene gel, 0.3%.Tell your doctor about all the medicines you take, including prescription and non-prescription medicines, vitamins and herbal supplements.Especially tell your doctor if you use any other medicine for acne. Using adapalene gel, 0.3% with topical medicines that contain sulfur, resorcinol or salicylic acid may cause skin irritation.Know the medicines you take. Keep a list of them to show your doctor and pharmacist when you get a new medicine.How should I use adapalene gel, 0.3%?Use adapalene gel, 0.3% exactly as your doctor tells you to use it. Adapalene gel, 0.3% is for skin use only. Do not use adapalene gel, 0.3% in or on your mouth, eyes, or vagina.Apply adapalene gel, 0.3% 1 time a day. Do not use more adapalene gel, 0.3% than you need to cover the treatment area. Using too much adapalene gel, 0.3% or using it more than 1 time a day may increase your chance of skin irritation.Applying adapalene gel, 0.3%:Wash the area where adapalene gel, 0.3% will be applied with a soap that does not contain a medicine and pat dry.Adapalene gel, 0.3% comes in a tube and a pump. If you have been prescribed the:Tube: Squeeze a small amount onto your fingertips and spread a thin layer over the entire face and any other affected areas.Pump: Depress the pump to dispense a small amount of adapalene gel, 0.3% and spread a thin layer over the entire face and any other affected area.What should I avoid while using adapalene gel, 0.3%?You should avoid spending time in sunlight or artificial sunlight, such as tanning beds or sunlamps. Adapalene gel, 0.3% can make your skin sensitive to sun and the light from tanning beds and sunlamps. You should wear sunscreen and wear a hat and clothes that cover the areas treated with adapalene gel, 0.3% if you have to be in sunlight.You should avoid weather extremes such as wind and cold as this may cause irritation to your skin.You should avoid applying adapalene gel, 0.3% to cuts, abrasions and sunburned skin.You should avoid skin products that may dry or irritate your skin such as harsh soaps, astringents, cosmetics that have strong skin drying effects and products containing high levels of alcohol.You should avoid the use of "waxing" as a hair removal method on skin treated with adapalene gel, 0.3%.What are the possible side effects of adapalene gel, 0.3%?Adapalene gel, 0.3% may cause serious side effects including:Local skin reactions. Local skin reactions are most likely to happen during the first 4 weeks of treatment and usually lessen with continued use of adapalene gel, 0.3%. Signs and symptoms of local skin reaction include:RednessDrynessScalingStinging or burningAllergic reactions. Adapalene gel, 0.3% may cause an allergic reaction that may require medical treatment. Stop using adapalene gel, 0.3% and tell your doctor right away if you have any of these symptoms of an allergic reaction:skin rash, itching or hivestrouble breathing or chest painswelling of your face, eyes, lips, tongue or throatYou may use a moisturizer for relief of dry skin or irritation, however you should avoid products that contain alpha hydroxy or glycolic acid.The most common side effects of adapalene gel, 0.3% are:  skin pain  skin peeling  sunburnTell your doctor if you have any side effect that bothers you or that does not go away.These are not all the possible side effects of adapalene gel, 0.3%. For more information, ask your doctor or pharmacist.Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.How should I store adapalene gel, 0.3%?  Store adapalene gel, 0.3% at room temperature between 68°F to 77°F (20° C to 25°C).  Do not freeze adapalene gel, 0.3%.Keep adapalene gel, 0.3% and all medicines out of the reach of children.General information about adapalene gel, 0.3%Medicines are sometimes prescribed for purposes other than those listed in a Patient Information Leaflet. Do not use adapalene gel, 0.3% for a condition for which it was not prescribed. Do not give adapalene gel, 0.3% to other people, even if they have the same symptoms you have. It may harm them.This Patient Information leaflet summarizes the most important information about adapalene gel, 0.3%. If you would like more information, talk with your doctor. You can also ask your doctor or pharmacist for information about adapalene gel, 0.3% that is written for health professionals.What are the ingredients in adapalene gel, 0.3%?Active ingredient: adapaleneInactive ingredients: carbopol 980, edetate disodium, methylparaben, poloxamer 124, propylene glycol, purified water and sodium hydroxide. May contain hydrochloric acid for pH adjustment.This Patient Information has been approved by the U.S. Food and Drug Administration.Manufactured by: Aleor Dermaceuticals Ltd., Karakhadi, Vadodara 391450, India.Mfg. Lic. No.: G/25/2216Manufactured for: Aleor Dermaceuticals Ltd., Karakhadi, Vadodara 391450, India.Revised: 6/2020

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