Label: MEMBERS MARK HYDROCORTISONE- hydrocortisone cream
- NDC Code(s): 68196-973-16, 68196-973-34
- Packager: Sam's West Inc
- Category: HUMAN OTC DRUG LABEL
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 October 25, 2021
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
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Uses
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- temporarily relieves itching associated with minor skin irritations, inflammation, and rashes due to:
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- eczema
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- psoriasis
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- poison ivy, oak, sumac
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- insect bites
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- detergents
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- jewelry
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- cosmetics
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- soaps
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- seborrheic dermatitis
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- temporarily relieves external anal and genital itching
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- other uses of this product should be only under the advice and supervision of a doctor
Do not use
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- in the genital area if you have a vaginal discharge. Ask a doctor.
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- for the treatment of diaper rash. Ask a doctor.
When using this product
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- avoid contact with the eyes
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- do not use more than directed unless told to do so by a doctor
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- do not put directly into the rectum by using fingers or any mechanical device or applicator
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Directions
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- for itching of skin irritation, inflammation, and rashes:
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- adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
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- children under 2 years of age: do not use, ask a doctor
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- for external anal and genital itching, adults:
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- when practical, clean the affected area with mild soap and warm water and rinse thoroughly
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- gently dry by patting or blotting with toilet tissue or a soft cloth before applying
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- apply to affected area not more than 3 to 4 times daily
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- children under 12 years of age: ask a doctor
- Other information
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Inactive ingredients
aloe barbadensis leaf juice, aluminum sulfate, calcium acetate, cetearyl alcohol, cetyl alcohol, cholecalciferol, dextrin, glycerin, isopropyl palmitate, light mineral oil, maltodextrin, methylparaben, propylene glycol, propylparaben, purified water, retinyl palmitate, sodium cetearyl sulfate, sodium lauryl sulfate, tocopherol, white petrolatum, white wax, zea mays (corn) oil
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Principal Display Panel
Compare to Cortizone-10® Plus active ingredient
FAST ITCH RELIEF
PLUS 10 HEALING MOISTURIZERS
MAXIMUM STRENGTH
Hydrocortisone 1% Plus
ANTI-ITCH CREAM
ULTRA MOISTURIZING ITCH RELIEF
Eczema & Psoriasis
Skin Irritations
Dry, Itchy Skin
Inflammation & Redness
Lasts 10 Hours
Strongest Itch Medicine without a Prescription
4 -2 OZ (56g) Tubes, Total 8 OZ (224g)
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INGREDIENTS AND APPEARANCE
MEMBERS MARK HYDROCORTISONE
hydrocortisone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68196-973 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 1 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ALUMINUM SULFATE (UNII: 34S289N54E) CALCIUM ACETATE (UNII: Y882YXF34X) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ALCOHOL (UNII: 936JST6JCN) CHOLECALCIFEROL (UNII: 1C6V77QF41) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) LIGHT MINERAL OIL (UNII: N6K5787QVP) MALTODEXTRIN (UNII: 7CVR7L4A2D) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B) SODIUM LAURYL SULFATE (UNII: 368GB5141J) TOCOPHEROL (UNII: R0ZB2556P8) PETROLATUM (UNII: 4T6H12BN9U) WHITE WAX (UNII: 7G1J5DA97F) CORN OIL (UNII: 8470G57WFM) ICODEXTRIN (UNII: 2NX48Z0A9G) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68196-973-34 4 in 1 CARTON 05/30/2019 1 NDC:68196-973-16 56 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 05/30/2019 Labeler - Sam's West Inc (051957769)