Label: HYDROCORTISONE- hydrocortisone continuous spray aerosol, spray
- NDC Code(s): 49035-011-40
- Packager: Wal-Mart Stores Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
-
Uses
For the temporary relief of itching associated with minor skin irritations, inframtation, and rashes due to:
- eczema
- insect bites
- poison ivy
- poison oak
- poison sumac
- soaps
- jewelry
- detergents
- cosmetics
- seborrheic dermatitis
- psoriasis
- other uses of this product should be only under the advice and supervision of a doctor
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Warnings
For external use only.
Flammable:
Keep away from heat, sparks and open flame, Contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120 F. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
Do not use
- for external genital, vaginal or anal itching
- with other hydrocortisone product unless consulted by a doctor
- in or near the eyes
- for diaper rash
When using this product
- avoid contact with eyes
- if product gets into the eye, flush with water for 15 minutes
- Directions
- Inactive ingredients
- Questions?
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
HYDROCORTISONE
hydrocortisone continuous spray aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 1.13 g in 113 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) OAT (UNII: Z6J799EAJK) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM (UNII: 7FLD91C86K) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) GLYCERIN (UNII: PDC6A3C0OX) MALTODEXTRIN (UNII: 7CVR7L4A2D) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) METHYL GLUCETH-20 (UNII: J3QD0LD11P) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) ALCOHOL (UNII: 3K9958V90M) SODIUM CITRATE (UNII: 1Q73Q2JULR) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-011-40 113 g in 1 CAN; Type 0: Not a Combination Product 04/15/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 04/15/2015 Labeler - Wal-Mart Stores Inc (051957769)