FIFTHPULSE CLOTRIMAZOLE ANTIFUNGAL- clotrimazole ointment

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Active ingredients

Clotrimazole USP 1% w/w

Purpose

Antifungal

Uses

• Cures athlete's foot (tine pedis) , jock itch (tines cruris), and ringworm (tinea corporis).
• Relieves the itching, irritation, redness, scaling and discomfort which can accompany these conditions.

Warnings

For external use only.

Do not use

on children 2 years of age unless directed by a doctor.

When using this product

avoid contact with eyes.

Stop use and ask a doctor if

• Irritation occurs
• There is no improvement within 4 weeks (for athlete's foot or ringworm) or within 2 weeks (for jock itch).

Keep this and all drugs out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away.

Directions

• Wash the affected area and dry thoroughly.
• Apply a thin layer over affected area twice daily (morning and night), or as directed by a doctor.
• Supervise children in the use of this product.
• For athelete's foot, pay special attention to the spaces between the toes; wear well-fitting ventilated shoes, and changes shoes and socks at least once daily.
• For athelete's foot and ringworm, use daily for 4 weeks. For jock itch, use daily for weeks.
• If condition persists longer, consult a doctor.
• This product is not effective on the scalp or nails.

Other information

• Store at controlled room temperature 15° to 30° C (59° to 86°F)
• Close cap tightly after use.

Inactive ingredients

Alcohol, Butylated hydroxytoluene, Cetostearyl alcohol, Dimethyl sulfoxide, Edetate disodium, Ethylparaben, Glycerol, Mineral oil, Mono-and-di-glycerides, Petrolatum, Polyoxyethylene lauryl ether, Purified water.Mineral oil, Petrolatum

Questions or Comments?

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Package Labeling:

Package Labeling:

INGREDIENTS AND APPEARANCE

FIFTHPULSE CLOTRIMAZOLE ANTIFUNGAL 
clotrimazole ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87525-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65)	CLOTRIMAZOLE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ETHYLPARABEN (UNII: 14255EXE39)
GLYCERIN (UNII: PDC6A3C0OX)
MINERAL OIL (UNII: T5L8T28FGP)
PETROLATUM (UNII: 4T6H12BN9U)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87525-002-01	1 in 1 BOX	04/30/2026
1		28.4 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 87525-002-02	1 in 1 BOX	04/30/2026
2		113.4 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	04/30/2026

Labeler - WeCare Products LLC (085508446)

Registrant - WeCare Products LLC (085508446)