FDA Label for Enstilar

1 Indications And Usage

Enstilar^® (calcipotriene and betamethasone dipropionate) Foam is indicated for the topical treatment of plaque psoriasis in patients 18 years of age and older.

2 Dosage And Administration

Instruct patients to shake can prior to using Enstilar^® Foam and to wash their hands after applying the product.

Apply Enstilar^® Foam to affected areas once daily for up to 4 weeks. Rub in Enstilar^® Foam gently. Discontinue use when control is achieved.

Instruct patients not to use more than 60 g every 4 days.

Enstilar^® Foam should not be used with occlusive dressings unless directed by a physician. Enstilar^® Foam is not for oral, ophthalmic, or intravaginal use.

Avoid use on the face, groin, or axillae, or if skin atrophy is present at the treatment site.

3 Dosage Forms And Strengths

Foam, 0.005%/0.064%

Enstilar^® Foam is a white to off-white opalescent liquid in a pressurized aluminum spray can with a continuous valve and actuator. At administration the product is a white to off-white foam after evaporation of the propellants. Each gram of Enstilar^® Foam contains 52.2 mcg calcipotriene hydrate (equivalent to 50 mcg of calcipotriene) and 0.643 mg of betamethasone dipropionate (equivalent to 0.5 mg of betamethasone).

4 Contraindications

None.

5.1 Flammability

The propellants in Enstilar^® Foam are flammable. Instruct the patient to avoid fire, flame, and smoking during and immediately following application.

5.2 Hypercalcemia And Hypercalciuria

Hypercalcemia and hypercalciuria have been observed with use of Enstilar^® Foam [see Clinical Pharmacology (12.2)]. If hypercalcaemia or hypercalciuria develop, discontinue treatment until parameters of calcium metabolism have normalized. The incidence of hypercalcemia and hypercalciuria following Enstilar^® Foam treatment of more than 4 weeks has not been evaluated.

5.3 Effects On Endocrine System

Systemic absorption of topical corticosteroids can produce reversible hypothalamic-pituitary-adrenal (HPA) axis suppression with the potential for clinical glucocorticosteroid insufficiency. This may occur during treatment or upon withdrawal of the topical corticosteroid. Factors that predispose a patient to HPA axis suppression include the use of high-potency steroids, large treatment surface areas, prolonged use, use of occlusive dressings, altered skin barrier, liver failure, and young age. Evaluation for HPA axis suppression may be done by using the adrenocorticotropic hormone (ACTH) stimulation test.

If HPA axis suppression is documented, gradually withdraw the drug, reduce the frequency of application, or substitute with a less potent corticosteroid.

Systemic effects of topical corticosteroids may also include Cushing's syndrome, hyperglycemia, and glucosuria.

Pediatric patients may be more susceptible to systemic toxicity due to their larger skin surface to body mass ratios [see Use in Specific Populations (8.3)].

Use of more than one corticosteroid-containing product at the same time may increase total systemic corticosteroid exposure.

5.4 Allergic Contact Dermatitis

Allergic contact dermatitis has been observed with topical calcipotriene and topical corticosteroids. Allergic contact dermatitis to a topical corticosteroid is usually diagnosed by observing a failure to heal rather than a clinical exacerbation. Corroborate such an observation with appropriate diagnostic patch testing.

5.5 Risks Of Ultraviolet Light Exposures

Patients who apply Enstilar^® Foam to exposed skin should avoid excessive exposure to either natural or artificial sunlight, including tanning booths, sun lamps, etc.

Physicians may wish to limit or avoid use of phototherapy in patients who use Enstilar^® Foam.

6.1 Clinical Trials Experience

Because clinical trials are conducted under widely varying conditions, adverse reaction 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.

The rates of adverse reactions given below were derived from three randomized, multicenter, prospective vehicle and/or active-controlled clinical trials in subjects with plaque psoriasis. Subjects applied study product once daily for 4 weeks, and the median weekly dose of Enstilar^® Foam was 24.8 g.

Adverse reactions reported in <1% of subjects treated with Enstilar^® Foam included: application site irritation, application site pruritus, folliculitis, skin hypopigmentation, hypercalcemia, urticaria, and exacerbation of psoriasis.

6.2 Postmarketing Experience

Because adverse 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.

Postmarketing reports for local adverse reactions to topical steroids include atrophy, striae, telangiectasia, dryness, perioral dermatitis, secondary infection and miliaria.

8.1 Pregnancy

Teratogenic Effects: Pregnancy Category C

There are no adequate and well-controlled studies in pregnant women. Pregnant women were excluded from the clinical studies conducted with Enstilar^® Foam. Enstilar^® Foam should be used during pregnancy only if the potential benefit to the patient justifies the potential risk to the fetus. Animal reproduction studies have not been conducted with Enstilar^® Foam. Enstilar^® Foam contains calcipotriene that has been shown to be fetotoxic and betamethasone dipropionate that has been shown to be teratogenic in animals when given systemically.

Teratogenicity studies with calcipotriene were performed by the oral route in rats and rabbits. In rabbits, increased maternal and fetal toxicity were noted at a dosage of 12 mcg/kg/day (144 mcg/m²/day); a dosage of 36 mcg/kg/day (432 mcg/m²/day) resulted in a significant increase in the incidence of incomplete ossification of the pubic bones and forelimb phalanges of fetuses. In a rat study, a dosage of 54 mcg/kg/day (324 mcg/m²/day) resulted in a significantly increased incidence of skeletal abnormalities (enlarged fontanelles and extra ribs). The enlarged fontanelles were most likely due to the effect of calcipotriene upon calcium metabolism. The estimated maternal and fetal no-adverse effect levels (NOAEL) in the rat (108 mcg/m²/day) and rabbit (48 mcg/m²/day) derived from oral studies are lower than the estimated maximum topical dose of calcipotriene in man (460 mcg/m²/day).

Corticosteroids have been shown to be teratogenic in laboratory animals when administered systemically at relatively low dosage levels.

Betamethasone dipropionate has been shown to be teratogenic in mice and rabbits when given by the subcutaneous route at dosages of 156 mcg/kg/day (468 mcg/m²/day) and 2.5 mcg/kg/day (30 mcg/m²/day), respectively. Those dose levels are lower than the estimated maximum topical dose in man (about 5,950 mcg/m²/day). The abnormalities observed included umbilical hernia, exencephaly and cleft palate.

Two oral peri- and post-natal development studies were conducted with rats:

Pregnant Wistar rats were dosed daily with calcipotriene at exposures of 0, 6, 18 or 54 mcg/kg/day from gestation day 15 through day 20 postpartum. No remarkable effects were observed on any parameter, including survival, behavior, body weight, litter parameters, or the ability to nurse or rear pups.

Betamethasone dipropionate was evaluated for effects when orally administered to pregnant rats from gestation day 6 through day 20 postpartum at dosages of 0, 100, 300, and 1000 mcg/kg/day. Mean maternal body weight was significantly reduced on gestation day 20 in animals dosed at 300 and 1000 mcg/kg/day. The mean duration of gestation was slightly, but statistically significantly, increased at 100, 300, and 1000 mcg/kg/day. The mean percentage of pups that survived to day 4 was reduced in relation to dosage. On lactation day 5, the percentage of pups with a reflex to right themselves when placed on their back was significantly reduced at 1000 mcg/kg/day. No effects on the ability of pups to learn were observed, and the ability of the offspring of treated rats to reproduce was not affected.

8.3 Nursing Mothers

Systemically administered corticosteroids appear in human milk and can suppress growth, interfere with endogenous corticosteroid production, or cause other untoward effects.

It is not known whether topically administered calcipotriene or corticosteroids could result in sufficient systemic absorption to produce detectable quantities in human milk.

Because many drugs are excreted in human milk, caution should be exercised when Enstilar^® Foam is administered to a nursing woman.

Instruct the patient not to use Enstilar^® Foam on the breast when nursing.

8.4 Pediatric Use

Safety and effectiveness of the use of Enstilar^® Foam in pediatric patients have not been studied. Because of a higher ratio of skin surface area to body mass, children under the age of 12 years are at particular risk of systemic adverse effects when they are treated with topical corticosteroids. They are, therefore, also at greater risk of HPA axis suppression and adrenal insufficiency with the use of topical corticosteroids. [see Warnings and Precautions (5.3)]

Cushing’s syndrome, linear growth retardation, delayed weight gain, and intracranial hypertension have been reported in pediatric patients treated with topical corticosteroids.

Local adverse reactions including striae have been reported with use of topical corticosteroids in pediatric patients.

8.5 Geriatric Use

Of the total number of subjects in the controlled clinical studies of Enstilar^® Foam in plaque psoriasis, 97 were 65 years or older, while 21 were 75 years or older.

No overall differences in safety or effectiveness of Enstilar^® Foam were observed between subjects in these subjects versus younger subjects, and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.

11 Description

Enstilar^® Foam contains calcipotriene hydrate and betamethasone dipropionate. It is intended for topical use only.

Calcipotriene hydrate is a synthetic vitamin D₃ analog.

Chemically, calcipotriene hydrate is 9,10-secochola-5,7,10(19),22-tetraene-1,3,24-triol,24-cyclo-propyl-,monohydrate, (1α,3ß,5Z,7E,22E,24S) with the empirical formula C₂₇H₄₀O₃,H₂O, a molecular weight of 430.6, and the following structural formula:

Calcipotriene hydrate is a white to almost white, crystalline compound.

Betamethasone dipropionate is a synthetic corticosteroid.

Betamethasone dipropionate has the chemical name pregna-1,4-diene-3,20-dione-9-fluoro-11-hydroxy-16-methyl-17,21-bis(1-oxypropoxy)-(11β,16β), with the empirical formula C₂₈H₃₇FO₇, a molecular weight of 504.6, and the following structural formula:

Betamethasone dipropionate is a white to almost white crystalline powder.

Enstilar^® Foam is a white to off-white opalescent liquid in a pressurized aluminum spray can with a continuous valve and actuator. The propellants used in Enstilar^® Foam are dimethyl ether and butane. At administration the product is a white to off-white foam after evaporation of the propellants. Each gram of Enstilar^® Foam contains 52.2 mcg calcipotriene hydrate (equivalent to 50 mcg of calcipotriene) and 0.643 mg of betamethasone dipropionate (equivalent to 0.5 mg of betamethasone) in a base of white petrolatum, polyoxypropylene stearyl ether, mineral oil, all-rac-alpha-tocopherol, and butylhydroxytoluene.

12.1 Mechanism Of Action

Enstilar^® Foam combines the pharmacological effects of calcipotriene hydrate as a synthetic vitamin D₃ analog and betamethasone dipropionate as a synthetic corticosteroid. However, while their pharmacologic and clinical effects are known, the exact mechanisms of their actions in plaque psoriasis are unknown.

12.2 Pharmacodynamics

Effects on Calcium Metabolism

Effects of once daily application of Enstilar^® Foam for 4 weeks on calcium metabolism in adult subjects (N=564) with plaque psoriasis were examined in three randomized, multicenter, prospective vehicle- and/or active-controlled clinical trials. Following once daily application of Enstilar^® Foam, elevated serum calcium levels outside the normal range were observed in 3 subjects. Elevated urinary calcium levels outside the normal range were observed in 17 subjects.

12.3 Pharmacokinetics

Absorption

The pharmacokinetics (PK) of Enstilar^® Foam was investigated in adult subjects (N = 35) with moderate to severe plaque psoriasis with a mean body surface area involvement of 17.5% and mean scalp involvement of 50.2%. Plasma concentrations of calcipotriene and betamethasone dipropionate and their main metabolites were measured after 4 weeks of once daily application of Enstilar^® Foam. Following application of a mean ± SD total weekly dose of 61.8 ± 27.7 grams of Enstilar^® Foam, calcipotriene was quantifiable in 1 of 35 (2.9%) subjects and its main metabolite, MC1080, in 3 of 35 (8.6%) subjects. For subjects with measurable concentrations, the maximal plasma concentrations (C_max) and area under the concentration curve until the last measured time point (AUC_last) for calcipotriene were 55.9 pg/mL and 82.5 pg*h/mL, respectively; and the mean ± SD C_max and AUC_last for MC1080 was 24.4 ± 1.9 pg/mL and 59.3 ± 5.4 pg*h/mL, respectively. Betamethasone dipropionate was quantifiable in 5 of 35 (14.3%) subjects and its main metabolite, betamethasone 17-propionate (B17P), was quantifiable in 27 of 35 (77.1%) subjects. The mean ± SD Cmax and AUClast for betamethasone dipropionate were 52.2 ± 19.7 pg/mL and 36.5 ± 27.4 pg*h/mL, respectively and for B17P were 147.9 ± 224.0 pg/mL and 683.6 ± 910.6 pg*h/mL, respectively. The clinical significance of these findings is unknown.

Metabolism

Calcipotriene:

Calcipotriene metabolism following systemic uptake is rapid and occurs in the liver. The primary metabolites of calcipotriene are less potent than the parent compound.

Calcipotriene is metabolized to MC1046 (the α,ß-unsaturated ketone analog of calcipotriene), which is metabolized further to MC1080 (a saturated ketone analog). MC1080 is the main metabolite in plasma. MC1080 is slowly metabolized to calcitroic acid.

Betamethasone dipropionate:

Betamethasone dipropionate is metabolized to betamethasone 17-propionate (B17P) and betamethasone, including the 6ß-hydroxy derivatives of those compounds by hydrolysis. B17P is the primary metabolite.

13.1 Carcinogenesis, Mutagenesis, Impairment Of Fertility

When calcipotriene was applied topically to mice for up to 24 months at dosages of 3, 10 and 30 mcg/kg/day (corresponding to 9, 30 and 90 mcg/m²/day), no significant changes in tumor incidence were observed when compared to control.

In a study in which albino hairless mice were exposed to both ultraviolet radiation (UVR) and topically applied calcipotriene, a reduction in the time required for UVR to induce the formation of skin tumors was observed (statistically significant in males only), suggesting that calcipotriene may enhance the effect of UVR to induce skin tumors.

A 104-week oral carcinogenicity study was conducted with calcipotriene in male and female rats at doses of 1, 5 and 15 mcg/kg/day (corresponding to dosages of approximately 6, 30, and 90 mcg/m²/day). Beginning week 71, the dosage for high-dose animals of both genders was reduced to 10 mcg/kg/day (corresponding to a dosage of approximately 60 mcg/m²/day). A treatment-related increase in benign C-cell adenomas was observed in the thyroid of females that received 15 mcg/kg/day. A treatment-related increase in benign pheochromocytomas was observed in the adrenal glands of males receiving 15 mcg/kg/day. No other statistically significant differences in tumor incidence were observed when compared to control. The relevance of these findings to patients is unknown.

When betamethasone dipropionate was applied topically to CD-1 mice for up to 24 months at dosages approximating 1.3, 4.2 and 8.5 mcg/kg/day in females, and 1.3, 4.2, and 12.9 mcg/kg/day in males (corresponding to dosages of up to approximately 26 mcg/m²/day and 39 mcg/m²/day, in females and males, respectively), no significant changes in tumor incidence were observed when compared to control.

When betamethasone dipropionate was administered via oral gavage to male and female Sprague Dawley rats for up to 24 months at dosages of 20, 60, and 200 mcg/kg/day (corresponding to dosages of approximately 120, 360, and 1200 mcg/m²/day), no significant changes in tumor incidence were observed when compared to control.

Calcipotriene did not elicit any genotoxic effects in the Ames mutagenicity assay, the mouse lymphoma TK locus assay, the human lymphocyte chromosome aberration test, or the mouse micronucleus test.

Betamethasone dipropionate did not elicit any genotoxic effects in the Ames mutagenicity assay, the mouse lymphoma TK locus assay, or in the rat micronucleus test.

Studies in rats with oral doses of up to 54 mcg/kg/day (324 mcg/m²/day) of calcipotriene indicated no impairment of fertility or general reproductive performance.

Studies in male rats at oral doses of up to 200 mcg/kg/day (1200 mcg/m²/day), and in female rats at oral doses of up to 1000 mcg/kg/day (6000 mcg/m²/day), of betamethasone dipropionate indicated no impairment of fertility.

14 Clinical Studies

Two multicenter, randomized, double-blind trials were conducted in subjects with plaque psoriasis. In Trial One, 302 subjects were randomized to 1 of 3 treatment groups: Enstilar^® Foam, betamethasone dipropionate in the same vehicle, or calcipotriene hydrate in the same vehicle. In Trial Two, 426 subjects were randomized to 1 of 2 treatment groups: Enstilar^® Foam or the vehicle alone. Baseline disease severity was graded using a 5-point Investigator’s Global Assessment (IGA). At baseline subjects scored “Mild”, “Moderate”, or “Severe”. The majority of subjects in both trials (76% and 75%) had disease of “Moderate” severity at baseline, 14% and 15% of subjects had disease of “Mild” severity at baseline and 10% of subjects had “Severe” disease at baseline in both trials. The extent of disease involvement assessed by mean body surface area was 7.1% (range 2 to 28%) and 7.5% (range 2 to 30%). In both trials, subjects were treated once daily for up to 4 weeks.

Efficacy was assessed with treatment success defined as the proportion of subjects at Week 4 who were “Clear” or “Almost Clear” according to the IGA. Subjects with “Mild” disease at baseline were required to be “Clear” to be considered a treatment success. Table 1 presents the efficacy results for these trials.

16.1 How Supplied

Enstilar^® Foam is a white to off-white opalescent liquid in a pressurized aluminum spray can with a continuous valve and actuator. At administration the product is a white to off-white foam after evaporation of the propellants.

Enstilar^® Foam is available as:

• 60 g can (NDC 50222-302-60)
• 120 g (2 cans of 60 g) (NDC 50222-302-66)

16.2 Storage

• Store Enstilar^® Foam at 20°- 25°C (68° -77°F); excursions permitted between 15°-30°C (59°-86°F). [See USP Controlled Room Temperature].
• Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120°F (49°C). Do not freeze.
• The product should be used within six months after it has been opened.

16.3 Handling

• Enstilar^® Foam is flammable; avoid heat, flame or smoking when using this product.

17 Patient Counseling Information

[Advise the patient to read the FDA-approved patient labeling (Patient Information and Instructions For Use)]

Inform patients of the following:

• Instruct patients to shake before use.
• Instruct patients not to use more than 60 g every 4 days.
• Discontinue therapy when control is achieved unless directed otherwise by the physician.
• Avoid use of Enstilar^® Foam on the face, underarms, groin or eyes. If this medicine gets on face or in mouth or eyes, wash area right away.
• Wash hands after application.
• Do not occlude the treatment area with a bandage or other covering unless directed by the physician. Instruct the patients not to use other products containing calcipotriene or a corticosteroid with Enstilar^® Foam without first talking to the physician.
• Instruct patients who use Enstilar^® Foam to avoid excessive exposure to either natural or artificial sunlight (including tanning booths, sun lamps, etc.). Physicians may wish to limit or avoid use of phototherapy in patients who use Enstilar^® Foam.
• Enstilar^® Foam is flammable; avoid heat, flame, or smoking when applying this medication.
• The foam can be sprayed holding the can in any orientation except horizontally.

Manufactured by:

LEO Laboratories Ltd.

285 Cashel Road

Dublin 12, Ireland

or

Colep Laupheim GmbH & Co. KG

Fockestraße 12

88471 Laupheim

Germany (DE)

Distributed by:

LEO Pharma Inc.

Seven Giralda Farms

Madison, NJ 07940, USA

Patient Information Enstilar® [En-Still-Ar]  (Calcipotriene And Betamethasone Dipropionate) Foam, 0.005%/0.064%

Important information:

Enstilar^® Foam is for use on the skin only (topical use). Do not get Enstilar^® Foam in your mouth, eyes, or vagina.

There are other medicines that contain the same medicine that is in Enstilar^® Foam and are used to treat plaque psoriasis. Do not use other products containing calcipotriene or a corticosteroid medicine with Enstilar^® Foam without talking to your doctor first.

What is Enstilar^® Foam?
Enstilar^® Foam is a prescription medicine that is used on the skin only (topical use) to treat plaque psoriasis in adults 18 years of age and older.

The safety and effectiveness of Enstilar^® Foam has not been studied in children.

Before using Enstilar^® Foam, tell your doctor about all of your health conditions, including if you:

• have a calcium metabolism disorder
• are getting phototherapy treatments (light therapy) for your psoriasis.
• are pregnant or plan to become pregnant. It is not known if Enstilar^® Foam can harm your unborn baby.
• are breastfeeding or plan to breastfeed. It is not known if Enstilar^® Foam passes into your breast milk. Do not use Enstilar^® Foam on your breast if you breastfeed.

Tell your doctor about all the medicines you take, including prescription and over-the-counter medicines, vitamins and herbal supplements.

How should I use Enstilar^® Foam?

See the “Instructions for Use” for detailed information about the right way to use Enstilar^® Foam.

• Use Enstilar^® Foam exactly as your doctor tells you to use it.
• Do not use more than 60 grams of Enstilar^® Foam every 4 days.
• Do not use Enstilar^® Foam longer than prescribed. Using too much Enstilar^® Foam, or using it too often, or for too long can increase your risk for having serious side effects.
• Apply Enstilar^® Foam to the affected areas of your skin 1 time a day for up to 4 weeks. You should stop treatment when your plaque psoriasis is under control unless your doctor gives you other instructions.
• Shake the Enstilar^® Foam can before you use it.
• Avoid using Enstilar^® Foam on your face, groin, or under your arms, or if you have thinning of your skin (atrophy) at the treatment site.
• If you accidentally get Enstilar^® Foam on the face, in the mouth or in the eyes, wash the area with water right away.
• Wash your hands after using Enstilar^® Foam unless you are using the medicine to treat your hands.
• Do not bandage or tightly cover the treated skin area, unless instructed by your doctor.
• Enstilar^® Foam is flammable. Avoid heat, flame, or smoking during and right after applying.

What should I avoid while using Enstilar^® Foam?
Avoid spending a long time in the sunlight. Avoid tanning booths and sunlamps.

What are the possible side effects of Enstilar^® Foam?

Enstilar^® Foam may cause serious side effects, including:

• too much calcium in your blood and urine. Your doctor may tell you to stop using Enstilar^® Foam until your calcium levels become normal.
• adrenal gland problems

Your doctor may do blood and urine tests to check your calcium levels and adrenal gland function while you are using Enstilar^® Foam.

• skin problems, including reactions where Enstilar^® Foam is applied, and allergic reactions (allergic contact dermatitis)

The most common side effects of Enstilar^® Foam include:

• irritation
• itching
• inflammation
• changes in skin color
• rash
• worsening of your psoriasis

Call your doctor about any side effect that bothers you or that does not go away.

These are not all of the possible side effects of Enstilar^® Foam. 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 Enstilar^® Foam?

• Store Enstilar^® Foam at room temperature between  68°F to 77°F (20°C to 25°C).
• Do not expose Enstilar^® Foam to heat or store at temperatures above 120°F (49°C).
• Do not puncture or burn the Enstilar^® Foam can.
• Do not freeze Enstilar^® Foam.
• Enstilar^® Foam has an expiration date (exp.) marked on the can. Do not use after this date.
• Use Enstilar^® Foam within 6 months after it has been opened.

Keep Enstilar^® Foam and all medicines out of the reach of children.

General information about the safe and effective use of Enstilar^® Foam.
Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use Enstilar^® Foam for a condition for which it was not prescribed. Do not give Enstilar^® Foam to other people, even if they have the same symptoms you have. It may harm them. You can ask your doctor or pharmacist for information about Enstilar^® Foam that is written for health professionals.

What are the ingredients in Enstilar^® Foam?
Active ingredients: calcipotriene hydrate and betamethasone dipropionate.
Inactive ingredients: white petrolatum, polyoxypropylene stearyl ether, mineral oil, all-rac-alpha-tocopherol, and butylhydroxytoluene.

Propellants: dimethyl ether and butane.

Manufactured by: LEO Laboratories Ltd., 285 Cashel Road, Dublin 12, Ireland or Colep Laupheim GmbH & Co. KG, Fockestraße 12, 88471 Laupheim, Germany (DE)

Distributed by: LEO Pharma Inc., Seven Giralda Farms, Madison, NJ 07940, USA

This Patient Information has been approved by the U.S. Food and Drug Administration. Issued: 06/2017

Instructions For Use Enstilar® (Calcipotriene And Betamethasone Dipropionate) Foam, 0.005%/0.064%

Read the Patient Information and Instructions for Use before you use Enstilar^® Foam.

Important information: For skin use only (topical use). Do not get Enstilar^® Foam in your mouth, eyes or vagina. If you accidentally get Enstilar^® Foam on the face, in the mouth or in the eyes, wash the area with water right away. Do not swallow Enstilar^® Foam.

How to apply ENSTILAR^® Foam:

Follow your doctor’s instructions on how much Enstilar^® Foam to use and where to use it.

This Instructions for Use has been approved by the U.S. Food and Drug Administration.

Manufactured by:

LEO Laboratories Ltd.
285 Cashel Road
Dublin 12, Ireland

or

Colep Laupheim GmbH & Co. KG

Fockestraße 12

88471 Laupheim

Germany (DE)

Distributed by:

LEO Pharma Inc.

Seven Giralda Farms

Madison, NJ 07940, USA

Issued: 06/2017

Principal Display Panel For Enstilar® (Calcipotriene And Betamethasone Dipropionate) Foam, 0.005%/0.064%

NDC 50222-302-60

Rx only

ENSTILAR^®

(calcipotriene and betamethasone dipropionate) Foam

0.005%/0.064%

Shake before Use

For Topical Use Only

Not for ophthalmic, oral or intravaginal use

Net Wt. 60 g

NDC 50222-302-66

Rx only

ENSTILAR^®

(calcipotriene and betamethasone dipropionate) Foam

0.005%/0.064%

Shake before Use

For Topical Use Only 

Not for ophthalmic, oral or intravaginal use

Net Wt. 120 g

(2 cans of 60 g)

Principal Display Panel For Enstilar® (Calcipotriene And Betamethasone Dipropionate) Foam, 0.005%/0.064%Physician Sample

NDC 50222-302-91

Rx only

ENSTILAR^®

(calcipotriene and betamethasone dipropionate) Foam

0.005%/0.064%

Physician's Sample - Not For Sale

Shake before Use

For Topical Use Only

Not for ophthalmic, oral or intravaginal use

Net Wt. 60 g