These highlights do not include all the information needed to use ACANYA Gel safely and effectively. See full prescribing information for ACANYA Gel.   ACANYA® (clindamycin phosphate and benzoyl peroxide) gel, 1.2%/2.5%, for topical useInitial U.S. Approval: 2000

These highlights do not include all the information needed to use ACANYA Gel safely and effectively. See full prescribing information for ACANYA Gel.   ACANYA® (clindamycin phosphate and benzoyl peroxide) gel, 1.2%/2.5%, for topical useInitial U.S. Approval: 2000

Drug Labeling and Warnings

Drug Details

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ACANYA- clindamycin phosphate and benzoyl peroxide gel 
Bausch Health US, LLC

----------

HIGHLIGHTS OF PRESCRIBING INFORMATION

These highlights do not include all the information needed to use ACANYA Gel safely and effectively. See full prescribing information for ACANYA Gel.
 
ACANYA® (clindamycin phosphate and benzoyl peroxide) gel, 1.2%/2.5%, for topical use
Initial U.S. Approval: 2000

INDICATIONS AND USAGE

ACANYA Gel is a combination of clindamycin phosphate (a lincosamide antibacterial) and benzoyl peroxide indicated for the topical treatment of acne vulgaris in patients 12 years or older. (1)

DOSAGE AND ADMINISTRATION

  • Apply a pea-sized amount of ACANYA Gel to the face once daily. (2)
  • Not for oral, ophthalmic, or intravaginal use. (2)

DOSAGE FORMS AND STRENGTHS

Gel, 1.2% clindamycin phosphate/2.5% benzoyl peroxide (3)

CONTRAINDICATIONS

ACANYA Gel is contraindicated in:

  • Patients who have demonstrated hypersensitivity (e.g., anaphylaxis) to clindamycin, benzoyl peroxide, any components of the formulation, or lincomycin. (4.1)
  • Patients with a history of regional enteritis, ulcerative colitis, or antibiotic-associated colitis. (4.2)

WARNINGS AND PRECAUTIONS

  • Colitis: Orally and parenterally administered clindamycin has been associated with severe colitis, which may result in death. Diarrhea, bloody diarrhea, and colitis (including pseudomembranous colitis) have been reported with the use of topical and systemic clindamycin. ACANYA Gel should be discontinued if significant diarrhea occurs. (5.1)
  • Ultraviolet Light and Environmental Exposure: Minimize sun exposure following drug application. (5.2)

ADVERSE REACTIONS

The following selected adverse reactions occurred in less than 0.2% of patients: application site pain (0.1%); application site exfoliation (0.1%); and application site irritation (0.1%). (6.1)

To report SUSPECTED ADVERSE REACTIONS, contact Bausch Health US, LLC at 1-800-321-4576 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

DRUG INTERACTIONS

  • Avoid using ACANYA Gel in combination with topical or oral erythromycin-containing products because of its clindamycin component. (7.1)

See 17 for PATIENT COUNSELING INFORMATION and FDA-approved patient labeling.

Revised: 2/2020

FULL PRESCRIBING INFORMATION

1 INDICATIONS AND USAGE

ACANYA® Gel is indicated for the topical treatment of acne vulgaris in patients 12 years or older.

2 DOSAGE AND ADMINISTRATION

Before applying ACANYA Gel, wash your face gently with a mild soap, rinse with warm water, and pat your skin dry. Apply a pea-sized amount of ACANYA Gel to the face once daily. Avoid the eyes, mouth, mucous membranes, or areas of broken skin.

Use of ACANYA Gel beyond 12 weeks has not been evaluated.

Concomitant topical acne therapy should be used with caution because a possible cumulative irritancy effect may occur, especially with the use of peeling, desquamating, or abrasive agents.

ACANYA Gel is not for oral, ophthalmic, or intravaginal use.

3 DOSAGE FORMS AND STRENGTHS

Gel, 1.2%/2.5%

Each gram of ACANYA Gel contains 10 mg (1%) clindamycin as phosphate, and 25 mg (2.5%) benzoyl peroxide in a white to off-white, opaque, smooth gel.

4 CONTRAINDICATIONS

4.1 Hypersensitivity

ACANYA Gel is contraindicated in those individuals who have shown hypersensitivity to clindamycin, benzoyl peroxide, any components of the formulation, or lincomycin. Anaphylaxis, as well as allergic reactions leading to hospitalization, has been reported in postmarketing use with ACANYA Gel [see Postmarketing Experience (6.2)].

4.2 Colitis/Enteritis

ACANYA Gel is contraindicated in patients with a history of regional enteritis, ulcerative colitis, or antibiotic-associated colitis [see Warnings and Precautions (5.1)].

5 WARNINGS AND PRECAUTIONS

5.1 Colitis

Systemic absorption of clindamycin has been demonstrated following topical use of clindamycin. Diarrhea, bloody diarrhea, and colitis (including pseudomembranous colitis) have been reported with the use of topical and systemic clindamycin. When significant diarrhea occurs, ACANYA Gel should be discontinued.

Severe colitis has occurred following oral and parenteral administration of clindamycin with an onset of up to several weeks following cessation of therapy. Antiperistaltic agents such as opiates and diphenoxylate with atropine may prolong and/or worsen severe colitis. Severe colitis may result in death.

Studies indicate toxin(s) produced by Clostridia is one primary cause of antibiotic-associated colitis. The colitis is usually characterized by severe persistent diarrhea and severe abdominal cramps and may be associated with the passage of blood and mucus. Stool cultures for Clostridium difficile and stool assay for C. difficile toxin may be helpful diagnostically.

5.2 Ultraviolet Light and Environmental Exposure

Minimize sun exposure including use of tanning beds or sun lamps following drug application.

5.3 Concomitant Topical Medications

Concomitant topical acne therapy should be used with caution since a possible cumulative irritancy effect may occur, especially with the use of peeling, desquamating, or abrasive agents. If irritancy or dermatitis occurs, reduce frequency of application or temporarily interrupt treatment and resume once the irritation subsides. Treatment should be discontinued if the irritation persists.

6 ADVERSE REACTIONS

6.1 Clinical Trials Experience

Because clinical trials are conducted under widely varying conditions, adverse reactions observed in the clinical trials of a drug cannot always be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

The following selected adverse reactions occurred in less than 0.2% of subjects treated with ACANYA Gel: application site pain (0.1%); application site exfoliation (0.1%); and application site irritation (0.1%).

During clinical trials, subjects were assessed for local cutaneous signs and symptoms of erythema, scaling, itching, burning and stinging. Most local skin reactions increased and peaked around Week 4 and continually decreased over time reaching near baseline levels by Week 12. The percentage of subjects that had symptoms present before treatment, the maximum value recorded during treatment, and the percent with symptoms present at Week 12 are shown in Table 1.

Table 1: Percent of Subjects with Local Skin Reactions. Combined Results from the Two Phase 3 Trials (N = 773)
Before Treatment
(Baseline)
Maximum During
Treatment
End of Treatment
(Week 12)
MildMod.*SevereMildMod.*SevereMildMod.*Severe
  • * Mod. = Moderate
  •   Erythema

    22

    4

    0

    25

    5

    < 1

    15

    2

    0

      Scaling

    8

    < 1

    0

    18

    3

    0

    8

    1

    0

      Itching

    10

    2

    0

    15

    2

    0

    6

    < 1

    0

      Burning

    3

    < 1

    0

    8

    2

    0

    2

    < 1

    0

      Stinging

    2

    < 1

    0

    6

    1

    0

    1

    < 1

    0

    6.2 Postmarketing Experience

    Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

    Anaphylaxis, as well as allergic reactions leading to hospitalizations, has been reported in postmarketing use of products containing clindamycin/benzoyl peroxide.

    7 DRUG INTERACTIONS

    7.1 Erythromycin

    ACANYA Gel should not be used in combination with topical or oral erythromycin-containing products due to its clindamycin component. In vitro studies have shown antagonism between erythromycin and clindamycin. The clinical significance of this in vitro antagonism is not known.

    7.2 Neuromuscular Blocking Agents

    Clindamycin has been shown to have neuromuscular blocking properties that may enhance the action of other neuromuscular blocking agents. Therefore, ACANYA Gel should be used with caution in patients receiving such agents.

    8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    There are no available data on ACANYA Gel use in pregnant women to evaluate a drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. The limited published data on use of clindamycin in pregnant women with exposure during the first trimester are insufficient to inform a drug-associated risk of pregnancy-related adverse outcomes (see Data). In limited published clinical trials with pregnant women, the systemic administration of clindamycin during the second and third trimesters has not been associated with an increased frequency of major birth defects.

    In animal reproduction studies, clindamycin did not cause malformations or embryo-fetal development toxicity in pregnant rats and mice when administered during the period of organogenesis at systemic doses up to 240 times the maximum recommended human dose (MRHD) of 2.5 g ACANYA Gel, based on body surface area (BSA) comparisons (see Data).

    The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of major birth defects, loss, and other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 -4% and 15-20%, respectively.

    Data

    Human Data

    In limited published trials in pregnant women administered clindamycin during the first trimester of pregnancy, there was no difference in the rate of major birth defects reported among in utero exposed infants compared to unexposed infants. These data cannot definitely establish or exclude any clindamycin-associated risk during pregnancy.

    Animal Data

    Animal reproductive/developmental toxicity studies have not been conducted with ACANYA Gel or benzoyl peroxide. Developmental toxicity studies of clindamycin performed in pregnant rats and mice administered during the period of organogenesis at oral doses of up to 600 mg/kg/day (240 and 120 times the MRHD for, respectively, based on BSA comparisons) or subcutaneous doses of up to 200 mg/kg/day (80 and 40 times the MRHD for clindamycin, respectively, based on BSA comparisons) revealed no malformations or embryo-fetal development toxicity.

    8.2 Lactation

    Risk Summary

    There are no data on the presence of clindamycin or benzoyl peroxide in human milk, the effects on the breastfed child, or the effects on milk production following topical administration. However, clindamycin has been reported to be present in breast milk in small amounts following oral and parenteral administration. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for ACANYA Gel and any potential adverse effects on the breastfed child from ACANYA Gel or from the underlying maternal condition.

    Clinical Considerations

    If used during lactation and ACANYA Gel is applied to the chest, care should be taken to avoid accidental ingestion by the infant.

    8.4 Pediatric Use

    Safety and effectiveness of ACANYA Gel in pediatric patients under the age of 12 have not been evaluated.

    8.5 Geriatric Use

    Clinical trials of ACANYA Gel did not include sufficient numbers of subjects aged 65 and older to determine whether they respond differently from younger subjects.

    11 DESCRIPTION

    ACANYA (clindamycin phosphate and benzoyl peroxide) Gel, 1.2%/2.5% is a combination product with two active ingredients in a white to off-white, opaque, smooth, aqueous gel formulation intended for topical use. Clindamycin phosphate is a water-soluble ester of the semisynthetic antibiotic produced by a 7(S)-chloro-substitution of the 7(R)‑hydroxyl group of the parent antibiotic lincomycin.

    The chemical name for clindamycin phosphate is Methyl 7-chloro-6,7,8-trideoxy-6-(1-methyl-trans-4-propyl-L-2-pyrrolidinecarboxamido)-1-thio-L-threo-α-D-galacto-octopyranoside 2-(dihydrogen phosphate). The structural formula for clindamycin phosphate is represented below:

    Clindamycin phosphate:

    acanya-01.jpg

    Molecular Formula: C18H34ClN2O8PS          Molecular Weight: 504.97

    Benzoyl peroxide is an antibacterial and keratolytic agent. The structural formula for benzoyl peroxide is represented below:

    Benzoyl peroxide:

    acanya-02.jpg

    Molecular Formula: C14H10O4          Molecular Weight: 242.23

    ACANYA Gel contains the following inactive ingredients: purified water, carbomer 980, propylene glycol, and potassium hydroxide. Each gram of ACANYA Gel contains 1.2% of clindamycin phosphate which is equivalent to 1% clindamycin.

    12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Clindamycin: Clindamycin is a lincosamide antibacterial [see Microbiology (12.4)].

    Benzoyl Peroxide: Benzoyl peroxide is an oxidizing agent with bactericidal and keratolytic effects but the precise mechanism of action is unknown.

    12.3 Pharmacokinetics

    The systemic absorption of clindamycin was investigated in an open-label, multiple-dose trial in 16 adult subjects with moderate to severe acne vulgaris treated with 1 gram of ACANYA Gel applied to the face once daily for 30 days. Twelve subjects (75%) had at least one quantifiable clindamycin plasma concentration above the lower limit of quantification (LOQ = 0.5 ng/mL) on Day 1 or Day 30. On Day 1, the mean (± standard deviation) peak plasma concentration (Cmax) was 0.78 ± 0.22 ng/mL (n=9 with measurable concentrations), and the mean AUC0-t was 5.29 ± 0.81 h.ng/mL (n=4). On Day 30, the mean Cmax was 1.22 ± 0.88 ng/mL (n=10), and the mean AUC0-t was 8.42 ± 6.01 h.ng/mL (n=6). Clindamycin plasma concentrations were below LOQ in all subjects at 24 hours post-dose on the three tested days (Day 1, 15, and 30).

    Benzoyl peroxide has been shown to be absorbed by the skin where it is converted to benzoic acid.

    12.4 Microbiology

    Clindamycin binds to the 50S ribosomal subunits of susceptible bacteria and prevents elongation of peptide chains by interfering with peptidyl transfer, thereby suppressing bacterial protein synthesis.

    Clindamycin and benzoyl peroxide individually have been shown to have in vitro activity against Propionibacterium acnes, an organism which has been associated with acne vulgaris; however, the clinical significance of this activity against P. acnes is not known.

    P. acnes resistance to clindamycin has been documented. Resistance to clindamycin is often associated with resistance to erythromycin.

    13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Carcinogenicity, mutagenicity, and impairment of fertility testing of ACANYA Gel have not been performed.

    Benzoyl peroxide has been shown to be a tumor promoter and progression agent in a number of animal studies. Benzoyl peroxide in acetone at doses of 5 and 10 mg administered topically twice per week for 20 weeks induced skin tumors in transgenic Tg.AC mice. The clinical significance of this is unknown.

    Carcinogenicity studies have been conducted with a gel formulation containing 1% clindamycin and 5% benzoyl peroxide. In a 2-year dermal carcinogenicity study in mice, treatment with the gel formulation at doses of 900, 2700, and 15000 mg/kg/day (1.8, 5.4, and 30 times the MRHD for clindamycin and 3.6, 10.8, and 60 times the MRHD for benzoyl peroxide, respectively, based on BSA comparisons) did not cause any increase in tumors. However, topical treatment with a different gel formulation containing 1% clindamycin and 5% benzoyl peroxide at doses of 100, 500, and 2000 mg/kg/day caused a dose-dependent increase in the incidence of keratoacanthoma at the treated skin site of male rats in a 2-year dermal carcinogenicity study in rats. In an oral (gavage) carcinogenicity study in rats, treatment with the gel formulation at doses of 300, 900, and 3000 mg/kg/day (1.2, 3.6, and 12 times the MRHD for clindamycin and 2.4, 7.2, and 24 times the MRHD for benzoyl peroxide, respectively, based on BSA comparisons) for up to 97 weeks did not cause any increase in tumors.

    Clindamycin phosphate was not genotoxic in the human lymphocyte chromosome aberration assay. Benzoyl peroxide has been found to cause DNA strand breaks in a variety of mammalian cell types, to be mutagenic in S. typhimurium tests by some but not all investigators, and to cause sister chromatid exchanges in Chinese hamster ovary cells.

    Fertility studies have not been performed with ACANYA Gel or benzoyl peroxide, but fertility and mating ability have been studied with clindamycin. Fertility studies in rats treated orally with up to 300 mg/kg/day of clindamycin (approximately 120 times the MRHD for clindamycin, based on BSA comparisons) revealed no effects on fertility or mating ability.

    14 CLINICAL STUDIES

    The safety and efficacy of once daily use of ACANYA Gel were assessed in two 12-week multi-center, randomized, blinded trials in subjects 12 years and older with moderate to severe acne vulgaris. The two trials were identical in design and compared ACANYA Gel to clindamycin in the vehicle gel, benzoyl peroxide in the vehicle gel, and the vehicle gel alone.

    The co-primary efficacy variables were:

    • 1. Mean absolute change from baseline at Week 12 in:
      • 1. Inflammatory lesion counts
      • 2. Non-inflammatory lesion counts
    • 2. Percent of subjects who had a 2-grade improvement from baseline on an Evaluator's Global Severity (EGS) score.

    The EGS scoring scale used in all of the clinical trials for ACANYA Gel is as follows:

    GradeDescription

    Clear

    Normal, clear skin with no evidence of acne vulgaris

    Almost Clear

    Rare non-inflammatory lesions present, with rare non-inflamed papules (papules must be resolving and may be hyperpigmented, though not pink-red)

    Mild

    Some non-inflammatory lesions are present, with few inflammatory lesions (papules/pustules only; no nodulocystic lesions)

    Moderate

    Non-inflammatory lesions predominate, with multiple inflammatory lesions evident: several to many comedones and papules/pustules, and there may or may not be one small nodulo-cystic lesion

    Severe

    Inflammatory lesions are more apparent, many comedones and papules/pustules, there may or may not be a few nodulocystic lesions

    Very Severe

    Highly inflammatory lesions predominate, variable number of comedones, many papules/pustules and many nodulocystic lesions

    The results of Trial 1 at Week 12 are presented in Table 2:

    Table 2: Trial 1 Results
    Trial 1ACANYA Gel
    N = 399
    Clindamycin
    Gel
    N = 408
    Benzoyl
    Peroxide Gel
    N = 406
    Vehicle Gel
    N = 201

    EGSS Clear or Almost Clear

    115 (29%)

    84 (21%)

    76 (19%)

    29 (14%)

    2-grade reduction from

    baseline

    131 (33%)

    100 (25%)

    96 (24%)

    38 (19%)

    Inflammatory Lesions:

      Mean absolute change

    14.8

    12.2

    13.0

    9.0

      Mean percent (%) reduction

    55.0%

    47.1%

    49.3%

    34.5%

    Non-Inflammatory Lesions:

      Mean absolute change

    22.1

    17.9

    20.6

    13.2

      Mean percent (%) reduction

    45.3%

    38.0%

    40.2%

    28.6%

    The results of Trial 2 at Week 12 are presented in Table 3:

    Table 3: Trial 2 Results
    ACANYA GelClindamycin
    Gel
    Benzoyl
    Peroxide Gel
    Vehicle Gel
    Trial 2N = 398N = 404N = 403N = 194
    •   EGSS Clear or Almost Clear
    •   113 (28%)
    •   94 (23%)
    •   94 (23%)
    •   21 (11%)
    •   2-grade reduction from baseline
    •   147 (37%)
    •   114 (28%)
    •   114 (28%)
    •   27 (14%)
    •   Inflammatory Lesions:
    •   Mean absolute change
    •   13.7
    •   11.3
    •   11.2
    •   5.7
    •   Mean percent (%) reduction
    •   54.2%
    •   45.3%
    •   45.7%
    •   23.3%
    •   Non-Inflammatory Lesions:
    •   Mean absolute change
    •   19.0
    •   14.9
    •   15.2
    •   8.3
    •   Mean percent (%) reduction
    •   41.2%
    •   34.3%
    •   34.5%
    •   19.2%

    16 HOW SUPPLIED/STORAGE AND HANDLING

    16.1 How Supplied

    ACANYA Gel, 1.2%/2.5% is a white to off-white smooth gel is supplied as:

    16.2 Dispensing Instructions for the Pharmacist

    • Dispense ACANYA Gel with a 10-week expiration date.
    • Specify "Store at room temperature up to 25°C (77°F). Do not freeze."

    16.3 Storage and Handling

    • PHARMACIST: Prior to Dispensing: Store in a refrigerator, 2° to 8°C (36° to 46°F).
    • PATIENT: Store at room temperature at or below 25°C (77°F).
    • Protect from freezing.
    • Store pump upright.
    • Keep out of the reach of children.
    • Keep container tightly closed.

    17PATIENT COUNSELING INFORMATION

    Advise the patient to read the FDA-approved patient labeling (Patient Information).

    • Patients who develop allergic reactions such as severe swelling or shortness of breath should discontinue use and contact their physician immediately.
    • ACANYA Gel may cause irritation such as erythema, scaling, itching, or burning, especially when used in combination with other topical acne therapies.
    • Excessive or prolonged exposure to sunlight should be limited. To minimize exposure to sunlight, a hat or other clothing should be worn. Sunscreen may also be used.
    • ACANYA Gel may bleach hair or colored fabric.

    Distributed by:
    Bausch Health US, LLC

    Bridgewater, NJ 08807 USA

    Manufactured by:
    Bausch Health Companies Inc.
    Laval, Quebec H7L 4A8, Canada

    U.S. Patents: 8,288,434; 8,663,699; 8,895,070; 9,078,870 and 9,693,988


    Acanya is a trademark of Bausch Health Companies Inc. or its affiliates.
    © 2020 Bausch Health Companies Inc. or its affiliates

    Patient Package Insert

    ACANYA® (AH-CAN΄-YAH)
    (clindamycin phosphate and benzoyl peroxide) gel, 1.2%/2.5%

    Important information: ACANYA Gel is for use on skin only (topical use). Do not use ACANYA Gel in your mouth, eyes, or vagina.

    •   What is ACANYA Gel?

    ACANYA Gel is a prescription medicine used on the skin (topical) to treat acne vulgaris in people 12 years of age and older.

    •   It is not known if ACANYA Gel is safe and effective for use longer than 12 weeks.

    It is not known if ACANYA Gel is safe and effective in children under 12 years of age.

    Do not use ACANYA Gel if you have:

    • had an allergic reaction to clindamycin, benzoyl peroxide, lincomycin or any of the ingredients in ACANYA Gel. See the end of this leaflet for a complete list of ingredients in ACANYA Gel.
    • Crohn’s disease or ulcerative colitis.
    • had inflammation of the colon (colitis), or severe diarrhea with past antibiotic use.

    Talk with your doctor if you are not sure if you have any of the conditions listed above.

    Before using ACANYA Gel, tell your doctor about all of your medical conditions, including if you:

    • plan to have surgery. ACANYA Gel may affect how certain medicines work that may be given during surgery.
    • are pregnant or plan to become pregnant. It is not known if ACANYA Gel will harm your unborn baby.
    • are breastfeeding or plan to breastfeed. It is not known if ACANYA Gel passes into your breast milk. Clindamycin when taken by mouth or by injection has been reported to appear in breast milk. Talk to your doctor about the best way to feed your baby during treatment with ACANYA Gel.

    Tell your doctor about all the medicines you take, including prescription and over-the-counter medicines, vitamins and herbal supplements. ACANYA Gel may affect the way other medicines work and other medicines may affect how ACANYA Gel works.

    • Especially tell your doctor if you take medicine by mouth that contains erythromycin or use products on your skin that contain erythromycin. ACANYA Gel should not be used with products that contain erythromycin.
    • Tell your doctor about any skin products you use. Other skin and topical acne products may increase the irritation of your skin when used with ACANYA Gel.

    Know the medicines you take. Keep a list of them and show it to your doctor and pharmacist when you get a new medicine.

    How should I use ACANYA Gel?

    • Use ACANYA Gel exactly as your doctor tells you to use it. See the detailed “Instructions for Use” for directions about how to apply ACANYA Gel.
    • Your doctor will tell you how long to use ACANYA Gel.
    • Apply ACANYA Gel to your face 1 time each day.

    What should I avoid while using ACANYA Gel?

    • Limit your time in sunlight. You should avoid using tanning beds or sunlamps during treatment with ACANYA Gel. If you have to be in sunlight, wear a wide-brimmed hat or other protective clothing, and use sunscreen to cover the treated areas.
    • Avoid getting ACANYA Gel in your hair or on colored fabric. ACANYA Gel may bleach hair or colored fabric.

    What are possible side effects of ACANYA Gel?

    ACANYA Gel can cause serious side effects including:

    • Inflammation of the colon (colitis). Stop using ACANYA Gel and call your doctor right away if you have severe stomach (abdominal) cramps, watery diarrhea, or bloody diarrhea during treatment, and within several weeks after treatment with ACANYA Gel.
    • Allergic reactions. Stop using ACANYA Gel, call your doctor and get help right away if you have any of the following symptoms during treatment with ACANYA Gel:
    • severe itching
    • swelling of your face, eyes, lips, tongue or throat
    • trouble breathing

    The most common side effects of ACANYA Gel include application site pain, application site irritation including redness, itching, burning, and stinging. Stop using ACANYA Gel and call your doctor if you have a skin rash or your skin becomes very red, itchy or swollen. Talk to your doctor about any side effect that bothers you or that does not go away.

    These are not all of the possible side effects with ACANYA Gel.

    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 ACANYA Gel?

    • Store ACANYA Gel at room temperature at or below 77°F (25°C).
    • Do not freeze ACANYA Gel.
    • Throw away (discard) ACANYA Gel that has passed the expiration date.
    • Store pump upright.
    • Keep the container tightly closed.

    Keep ACANYA Gel and all medicines out of the reach of children.

    General information about the safe and effective use of ACANYA Gel.

    Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use ACANYA Gel for a condition for which it was not prescribed. Do not give ACANYA Gel to other people, even if they have the same condition you have. It may harm them. You can also ask your doctor or pharmacist for information about ACANYA Gel that is written for healthcare professionals.

    What are the ingredients in ACANYA Gel?

    Active Ingredients: clindamycin phosphate and benzoyl peroxide

    Inactive Ingredients: purified water, carbomer 980, propylene glycol, and potassium hydroxide


    Distributed by:
    Bausch Health US, LLC, Bridgewater, NJ 08807 USA

    Manufactured by: Bausch Health Companies Inc., Laval, Quebec H7L 4A8, Canada

    U.S. Patent Numbers: 8,288,434; 8,663,699; 8,895,070; 9,078,870 and 9,693,988
    Acanya is a trademark of Bausch Health Companies Inc. or its affiliates.

    © 2020 Bausch Health Companies Inc. or its affiliates

    For more information about ACANYA Gel, call 1-800-321-4576.

    This Patient Information has been approved by the U.S. Food and Drug Administration.

    Revised: 02/2020

    INSTRUCTIONS FOR USE

    ACANYA® (AH-CAN΄-YAH)
    (clindamycin phosphate and benzoyl peroxide) gel, 1.2%/2.5%

    Important Information: ACANYA Gel is for use on skin only (topical use). ACANYA Gel is not for use in your mouth, eyes or vagina.

    Read this Instructions for Use before you start using ACANYA Gel and each time you get a refill. There may be new information. This information does not take the place of talking with your doctor about your medical condition or treatment.

    • Apply ACANYA Gel to your face 1 time each day as prescribed.
    • Before you apply ACANYA Gel, wash your face gently with a mild soap, rinse with warm water, and pat your skin dry.
    • To apply ACANYA Gel to your face, use the pump to dispense one pea-sized amount of ACANYA Gel onto your fingertip. See Figure 1.
    • One pea-sized amount of ACANYA Gel should be enough to cover your entire face.
    figure-1

    Figure 1

    • Dot the one pea-sized amount of ACANYA Gel onto six areas of your face (chin, left cheek, right cheek, nose, left forehead, right forehead). See Figure 2.
    figure-2

    Figure 2

    • Spread the gel over your face and gently rub it in. It is important to spread the gel over your entire face. If your doctor tells you to put ACANYA Gel on other areas of your skin with acne, be sure to ask how much you should use.
    • Wash your hands with soap and water after applying ACANYA Gel.

    How should I store ACANYA Gel?

    • Store ACANYA Gel at room temperature at or below 77°F (25°C).
    • Do not freeze ACANYA Gel.
    • Throw away (discard) ACANYA Gel that has passed the expiration date.
    • Store pump upright.
    • Keep the container tightly closed.

    Keep ACANYA Gel and all medicines out of the reach of children.

    The Patient Information and Instructions for Use have been approved by the U.S. Food and Drug Administration.

    Issued: February 2020

    PRINCIPAL DISPLAY PANEL - 50 gram Carton

    NDC 13548-132-50

    Rx only

    ACANYA®
    (Clindamycin Phosphate and
    Benzoyl Peroxide) Gel, 1.2%/2.5%

    For Topical Use Only

    One premixed 50-gram pump dispensercarton.jpg

    ACANYA 
    clindamycin phosphate and benzoyl peroxide gel
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 13548-132
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Clindamycin Phosphate (UNII: EH6D7113I8) (Clindamycin - UNII:3U02EL437C) Clindamycin10 mg  in 1 g
    Benzoyl Peroxide (UNII: W9WZN9A0GM) (Benzoyl Peroxide - UNII:W9WZN9A0GM) Benzoyl Peroxide25 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    propylene glycol (UNII: 6DC9Q167V3)  
    potassium hydroxide (UNII: WZH3C48M4T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 13548-132-501 in 1 CARTON07/26/2010
    150 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA05081907/26/2010
    Labeler - Bausch Health US, LLC (831922468)
    Establishment
    NameAddressID/FEIBusiness Operations
    Contract Pharmaceuticals Limited Canada248761249MANUFACTURE(13548-132) , PACK(13548-132)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bausch Health Companies, Inc.245141858MANUFACTURE(13548-132) , PACK(13548-132)

    Revised: 2/2020
     
    Bausch Health US, LLC


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