Label: HYDROCORTISONE CONTINUOUS- hydrocortisone aerosol, spray
- NDC Code(s): 79481-0618-1
- Packager: Meijer Distribution Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 13, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
-
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
- jewelry
- detergents
- cosmetics
- seborrheic dermatitis
- psoriasis
- other uses of this product should be only under the advice and supervision of a doctor
-
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 ºF. 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 directed by a doctor
- in or near the eyes
- for diaper rash
When using this product
- avoid contact with the eyes
- if product gets into the eye, flush with water for 15 minutes
- Directions
- Inactive ingredients
- Questions ?
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
HYDROCORTISONE CONTINUOUS
hydrocortisone aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79481-0618 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 g Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) SODIUM CITRATE (UNII: 1Q73Q2JULR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ALOE VERA LEAF (UNII: ZY81Z83H0X) METHYL GLUCETH-20 (UNII: J3QD0LD11P) OAT (UNII: Z6J799EAJK) WATER (UNII: 059QF0KO0R) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) ALCOHOL (UNII: 3K9958V90M) MALTODEXTRIN (UNII: 7CVR7L4A2D) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79481-0618-1 113 g in 1 CAN; Type 0: Not a Combination Product 08/27/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 08/27/2023 Labeler - Meijer Distribution Inc. (006959555)