Label: MEIJER MAXIMUM STRENGTH ANTI-ITCH CREAM ULTRA MOISTURIZING FORMULA 1OZ- hydrocortisone cream
- NDC Code(s): 41250-584-28
- Packager: MEIJER, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 15, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
PURPOSE
Uses
temporarily relieves itching associated with minor skin irritations, inflammation, and rashes due to:
- eczema
- psoriasis
- jewelry
- insect bites
- soaps
- cosmetics
- detergents
- seborrheic dermatitis
- poison ivy, oak sumac
temporarily relieves external anal and genital itching
other uses of this product should only be under the advice and supervision of a doctor
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
-
INDICATIONS & USAGE
Directions
for itching of skin irritation, inflammation, and rashes:
- 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: ask a doctor
for external anal and genital itching, adults:
- when practical, clean the affected area with mild soap and warm water and rinse thoroughly
- gently dry by patting or blotting with toilet tissue or a soft cloth before applying
- apply to affected are not more than 3 to 4 times daily
- children under 12 years of age: ask a doctor
- DOSAGE & ADMINISTRATION
-
INACTIVE INGREDIENT
Inactive Ingredients .alpha.-tocopherol acetate, aloe vera leaf, aluminium sulfate octadecahydrate, calcium acetate monohydrate, cetostearyl alcohol, cetyl alcohol, corn oil, dextrin, glycerin, isopropyl palmitate, light mineral oil, maltodextrin, methylparaben, petrolatum, propylene glycol, propylparaben, purified water, sodium cetostearyl sulfate, sodium lauryl sulfate, vitamin a palmitate, white wax
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MEIJER MAXIMUM STRENGTH ANTI-ITCH CREAM ULTRA MOISTURIZING FORMULA 1OZ
hydrocortisone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-584 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 PROPYLPARABEN (UNII: Z8IX2SC1OH) SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B) WATER (UNII: 059QF0KO0R) WHITE WAX (UNII: 7G1J5DA97F) ALOE VERA LEAF (UNII: ZY81Z83H0X) CETYL ALCOHOL (UNII: 936JST6JCN) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) LIGHT MINERAL OIL (UNII: N6K5787QVP) ALUMINIUM SULFATE OCTADECAHYDRATE (UNII: TCS9L00G8F) CALCIUM ACETATE MONOHYDRATE (UNII: 7ZA48GIM5H) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERIN (UNII: PDC6A3C0OX) CORN OIL (UNII: 8470G57WFM) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM LAURYL SULFATE (UNII: 368GB5141J) MALTODEXTRIN (UNII: 7CVR7L4A2D) METHYLPARABEN (UNII: A2I8C7HI9T) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-584-28 1 in 1 CARTON 07/13/2020 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 not final part348 07/13/2020 Labeler - MEIJER, INC. (006959555)