ANTIFUNGAL- clotrimazole cream

Antifungal by

Drug Labeling and Warnings

Antifungal by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Clotrimazole USP 1%

Purpose

Antifungal

Uses

For the treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis)

Relieves itching, scaling, burning, redness, soreness, irritation, discomfort, and chafing associated with jock itch and itching, burning feet

Warnings

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

For external use only

Avoid contact with eyes

Stop use and ask a doctor if

Irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor for athlete's foot and ringworm.

Irritation occurs or if there is no improvement within 2 weeks, discontinue use and consult a doctor for jock itch.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away

Directions

Clean 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 athlete's foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. For athlete's foot and ringworm; use daily for 4 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 20°-25°C (68°-77°F)

Tamper evident. Do not use if seal is damaged.

Inactive ingredients

ceteth-20, cetostearyl alcohol, light mineral oil, methylparaben, propylene glycol, propylparaben, purified water, petrolatum

Label 1231-C

Label 1233-C

INGREDIENTS AND APPEARANCE

ANTIFUNGAL 
clotrimazole cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-727
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65)	CLOTRIMAZOLE	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
LIGHT MINERAL OIL (UNII: N6K5787QVP)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
METHYLPARABEN (UNII: A2I8C7HI9T)
PETROLATUM (UNII: 4T6H12BN9U)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
CETETH-20 (UNII: I835H2IHHX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-727-02	72 in 1 CASE	03/24/2026
1	NDC: 67777-727-01	28.4 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 67777-727-05	4 in 1 CASE	03/24/2026
2	NDC: 67777-727-04	6 in 1 BOX
2	NDC: 67777-727-03	113 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	03/24/2026

Labeler - Dynarex Corporation (008124539)