Label: NO MESS HYDROCORTISONE APPLICATOR- hydrocortisone liquid
- NDC Code(s): 0363-0358-12
- Packager: Walgreen Co.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 16, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only
Flammable: Keep away from fire or flame and heated surfaces
Do not use
- for the treatment of diaper rash. Consult a doctor.
- if you are allergic to any ingredient in the product
When using this product
- avoid contact with eyes
- do not use more than directed unless told to do so by a doctor
- Directions
- Other information
- Inactive ingredients
-
Principal Display Panel – 36 mL Carton Label
Walgreens
WALGREENS • PHARMACIST RECOMMENDED
Compare to the active ingredient in
Cortizone-10® Maximum Strength
Anti-Itch Liquid With Aloe††NO MESS
Hydrocortisone
ApplicatorHYDROCORTISONE 1% / ANTI-ITCH
+ Aloe
Fast Itch Relief
-
Maximum Strength without
a prescription* -
Relieves itch associated
with rashes, inflammation,
& minor skin irritations
1
APPLICATOR1.25 FL OZ (36 mL)
Aloe
NOT ACTUAL SIZE
-
Maximum Strength without
-
INGREDIENTS AND APPEARANCE
NO MESS HYDROCORTISONE APPLICATOR
hydrocortisone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0358 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) ALOE VERA LEAF (UNII: ZY81Z83H0X) OAT (UNII: Z6J799EAJK) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) 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) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0358-12 1 in 1 CARTON 02/16/2024 1 36 mL in 1 BOTTLE, WITH APPLICATOR; 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 02/16/2024 Labeler - Walgreen Co. (008965063) Registrant - NATURAL ESSENTIALS, INC. (947484713) Establishment Name Address ID/FEI Business Operations NATURAL ESSENTIALS, INC. 947484713 MANUFACTURE(0363-0358)