Label: DG HEALTH HYDROCORTISONE- hydrocortisone cream
- NDC Code(s): 55910-504-16
- Packager: Dolgencorp, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2024
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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
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Warnings
For external use only
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
DG™|health
Compare to the active ingredient of Cortizone•10® Plus
Maximum Strength
Hydrocortisone Cream 1%
Anti-Itch Cream
Plus 10 Moisturizers
Relieves Itch Fast
• Dry Skin
• Rashes
• Skin Irritation
• Eczema & Psoriasis
• Inflammation & Redness
LASTS 10 HOURS††
Enriched with Aloe
plus vitamins A & E
††When used as directed
NET WT. 2 OZ (56 g)
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INGREDIENTS AND APPEARANCE
DG HEALTH HYDROCORTISONE
hydrocortisone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-504 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:55910-504-16 1 in 1 CARTON 12/11/2020 1 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 Drug M017 12/11/2020 Labeler - Dolgencorp, LLC (068331990)