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NDC 59088-0244-07 CVS Feminine Intimate Powder 20 mg/g Details

CVS Feminine Intimate Powder 20 mg/g

CVS Feminine Intimate Powder is a TOPICAL POWDER in the HUMAN OTC DRUG category. It is labeled and distributed by PureTek Corporation. The primary component is MICONAZOLE NITRATE.

MedlinePlus Drug Summary

Topical miconazole is used to treat tinea corporis(ringworm; fungal skin infection that causes a red scaly rash on different parts of the body), tinea cruris (jock itch; fungal infection of the skin in the groin or buttocks), and tinea pedis (athlete's foot; fungal infection of the skin on the feet and between the toes). Miconazole is in a class of antifungal medications called imidazoles. It works by stopping the growth of fungi that cause infection. Not all products should be used to treat all of these conditions. Please read the label for each product to select the one to treat your condition.

Related Packages: 59088-0244-07
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Miconazole Topical

Product Information

NDC	59088-0244
Product ID	59088-244_a1d9a187-696c-a2f2-e053-2a95a90afc3e
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	CVS Feminine Intimate Powder
Proprietary Name Suffix	n/a
Non-Proprietary Name	Miconazole Nitrate
Product Type	HUMAN OTC DRUG
Dosage Form	POWDER
Route	TOPICAL
Active Ingredient Strength	20
Active Ingredient Units	mg/g
Substance Name	MICONAZOLE NITRATE
Labeler Name	PureTek Corporation
Pharmaceutical Class	Azole Antifungal [EPC], Azoles [CS]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part333C
Listing Certified Through	2024-12-31

Package

Package Images

NDC 59088-0244-07 (59088024407)

Pricing Information	N/A
NDC Package Code	59088-244-07
Billing NDC	59088024407
Package	85 g in 1 BOTTLE (59088-244-07)
Marketing Start Date	2019-05-31
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL eda5026e-d941-4fb8-a0c6-c70ea1d68532 Details

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS FEMININE INTIMATE POWDER

miconazole nitrate powder

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	20 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
KUKUI NUT OIL (UNII: TP11QR7B8R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
LEVOMENOL (UNII: 24WE03BX2T)
CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
NYLON-12 (UNII: 446U8J075B)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
STARCH, CORN (UNII: O8232NY3SJ)
GINGER (UNII: C5529G5JPQ)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:59088-244-07	85 g in 1 BOTTLE; Type 0: Not a Combination Product	05/31/2019

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

Labeler - PureTek Corporation (785961046)

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

Revised: 3/2020

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

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

Version: 2

Effective Time: 20200327