Label: HYDROCORTISONE- hydrocortisone spray spray
- NDC Code(s): 79481-9967-1
- Packager: Meijer Distribution Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 9, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
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Uses
for the temporary relief of itching associated with minor skin irritations, inflammation, and rashes due to:
- eczema
- insect bites
- poison ivy
- poison oak
- poison sumac
- soaps
- detergents
- cosmetics
- jewelry
- seborrheic dermatitis
- psoriasis
- other uses of this product should be only under the advice and supervision of a doctor
- Warnings
- Directions
- Other Information
- Inactive ingredients
- Questions ?
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INGREDIENTS AND APPEARANCE
HYDROCORTISONE
hydrocortisone spray sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79481-9967 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) MENTHYL LACTATE (UNII: 2BF9E65L7I) METHYL GLUCETH-20 (UNII: J3QD0LD11P) OAT (UNII: Z6J799EAJK) PROPANEDIOL (UNII: 5965N8W85T) SODIUM CITRATE (UNII: 1Q73Q2JULR) CITRIC ACID (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79481-9967-1 74 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 12/09/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 12/09/2024 Labeler - Meijer Distribution Inc. (006959555)