Label: EQUATE HYDROCORTIONE- 1% hydrocortisone cream
- NDC Code(s): 79903-211-01
- Packager: Walmart Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 8, 2024
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- Official Label (Printer Friendly)
- Drug Fact
- Active Ingredient
- Purpose
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Uses
For temporarily relief of itching associated with minor skin irritations, inflammation, and rashes due to:
■ eczema ■ psoriasis ■ poison ivy, oak, sumac ■ insect bites ■ detergents ■ jewelry ■ cosmetics
■ soaps ■ seborrheic dermatitis
Other uses of this product should only be under the advice and supervision of a doctor
- Warnings For external use only
- Do not use
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When using this product
- Avoid contact with the eyes
- Do not begin the use of any other hydrocortisone products unless you have consulted a doctor.
- For genital, feminine and anal itching do not exceed the recommended daily dose unless directed by a doctor, in case of bleeding , stop use and consult a doctor
- Do not put this product into the rectum by using fingers or any mechanical device or applicator.
- Stop use and ask a doctor if
- Keep out of the reach of children
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Directions
- adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
- children under 2 years of age: do not use, ask a doctor
- For external anal itching ; adults ; when practical cleanse the affected area with mild soap and warm water and rinse thoroughly or by patting or blotting with toilet tissue or a soft cloth before application of this product.Children under 12 years of age with external anal itching consult a doctor.
- Other information
- Inactive ingredients
- Principal Display Panel 1 oz
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INGREDIENTS AND APPEARANCE
EQUATE HYDROCORTIONE
1% hydrocortisone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-211 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE ACETATE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) PETROLATUM (UNII: 4T6H12BN9U) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM LAURYL SULFATE (UNII: 368GB5141J) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-211-01 1 in 1 CARTON 01/31/2024 1 28 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 M017 01/31/2024 Labeler - Walmart Inc. (051957769)