Label: CLOTRIMAZOLE CREAM 1%- clotrimazole cream
- NDC Code(s): 79503-105-30
- Packager: Ezricare Llc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 11, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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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 • there is no improvement within 2 weeks when used for the treatment of jock itch • there is no improvement within 4 weeks when used for athlete’s foot or ringworm
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Directions
• Clean the affected area and dry thoroughly. Apply a thin layer of cream 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 • For jock itch, use daily for 2 weeks • If condition persists longer, consult a doctor. This product is not effective on the scalp or nails
- Other information
- Inactive ingredients
- Questions or comments?
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SPL UNCLASSIFIED SECTION
Cures Most Athlete's Foot
Compared to the active ingredient in Lotrimin® AF*
Relieves Itching and Burning Sensation. Relieves from Cracking and Scaling. Greaseless and non-staining.
*This product is not affiliated with, manufactured by, or produced by the makers or owners of Lotrimin® AF
Distributed by:
EzriCare, LLC
Lakewood, NJ
www.EzriCare.com
Made in India
- Packaging
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INGREDIENTS AND APPEARANCE
CLOTRIMAZOLE CREAM 1%
clotrimazole creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79503-105 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 CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) METHYLPARABEN (UNII: A2I8C7HI9T) MINERAL OIL (UNII: T5L8T28FGP) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) WHITE PETROLATUM (UNII: B6E5W8RQJ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79503-105-30 1 in 1 CARTON 08/19/2021 07/01/2025 1 30 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 08/19/2021 07/01/2025 Labeler - Ezricare Llc (117573818)