CVS Feminine Intimate Powder

Dosage form: powder
Ingredients: MICONAZOLE NITRATE 20mg in 1g
Labeler: PureTek Corporation
NDC code: 59088-244

Medically reviewed by Drugs.com. Last updated on Mar 18, 2024.

Drug Facts

Active ingredient
Miconazole Nitrate 2%

Purposes

Antifungal

Uses

for the treatment and relief of external genital itching
relieves itching, scaling, cracking, burning, redness, soreness, irritation, discomfort and chafing associated with external genital itching

Warnings

For external use only

Do not use on children under 2 years of age unless directed by a doctor.

When using this product avoid contact with the eyes.

Stop use and ask a doctor if

irritation occurs or if there is no improvement within 2 weeks

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

clean the affected area and dry thoroughly
apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor
supervise children in the use of this product

Other information

store between 59°-86°F
lightly shake bottle to loosen settled powder

Inactive ingredients

Aleurites Moluccana Seed Oil, Aloe Barbadensis (Aloe Vera) Leaf Juice Powder, Bisabolol, Carthamus Tinctorius (Safflower) Oleosomes, Fragrance, Nylon-12, Silica, Sodium Benzoate, Sodium Hyaluronate, Zea Mays (Corn) Starch, Zingiber Officinale (Ginger) Root Extract.

CVS FEMININE INTIMATE POWDER
miconazole nitrate powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:59088-244
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (MICONAZOLE)	MICONAZOLE NITRATE	20 mg in 1 g

Inactive Ingredients
Ingredient Name	Strength
KUKUI NUT OIL
ALOE VERA LEAF
LEVOMENOL
CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES
NYLON-12
SILICON DIOXIDE
SODIUM BENZOATE
HYALURONATE SODIUM
STARCH, CORN
GINGER

Packaging
#	Item Code	Package Description
1	NDC:59088-244-07	85 g in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	05/31/2019

Labeler - PureTek Corporation (785961046)

Establishment
Name	Address	ID/FEI	Operations
PureTek Corporation		785961046	manufacture(59088-244)

Document Id: a1d9a187-696c-a2f2-e053-2a95a90afc3e

Set id: eda5026e-d941-4fb8-a0c6-c70ea1d68532

Version: 2

Effective Time: 20200327

PureTek Corporation

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer