Label: DG HEALTH HYDROCORTISONE- hydrocortisone lotion
- NDC Code(s): 55910-646-25
- Packager: Dolgencorp, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 31, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Directions
- Other information
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Inactive ingredients
aloe barbadensis leaf juice, avena sativa (oat) kernel extract, bisabolol, boswellia serrata gum, butyrospermum parkii (shea butter) extract, cetyl alcohol, dextrin, dimethicone, dipropylene glycol, edetate disodium, glycerin, glyceryl stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, magnesium ascorbyl phosphate, maltodextrin, methyl gluceth-20, methylparaben, petrolatum, phenoxyethanol, polysorbate 60, propylparaben, purified water, retinyl palmitate, sodium citrate, tocopheryl acetate, zingiber officinale (ginger) root extract
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Package/Label Principal Display Panel
Compare to the active ingredient of Cortizone-10® Intensive Healing Lotion
Maximum Strength
Hydrocortisone 1% Lotion
Anti-Itch Lotion
Eczema and Itchy, Dry Skin
Intensive Healing Lotion
#1 Doctor recommended itch relief active ingredient
Clinically proven to moisturize 24 hours
With Botanicals and Antioxidant vitamins A, C & E
7 intensive moisturizers
NET WT 3.5 OZ (99 g)
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INGREDIENTS AND APPEARANCE
DG HEALTH HYDROCORTISONE
hydrocortisone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-646 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) OAT (UNII: Z6J799EAJK) LEVOMENOL (UNII: 24WE03BX2T) INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) CETYL ALCOHOL (UNII: 936JST6JCN) ICODEXTRIN (UNII: 2NX48Z0A9G) DIMETHICONE (UNII: 92RU3N3Y1O) DIPROPYLENE GLYCOL (UNII: E107L85C40) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ISOHEXADECANE (UNII: 918X1OUF1E) MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5) MALTODEXTRIN (UNII: 7CVR7L4A2D) METHYL GLUCETH-20 (UNII: J3QD0LD11P) METHYLPARABEN (UNII: A2I8C7HI9T) PETROLATUM (UNII: 4T6H12BN9U) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 60 (UNII: CAL22UVI4M) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) GINGER (UNII: C5529G5JPQ) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-646-25 1 in 1 CARTON 12/28/2020 1 99 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 12/28/2020 Labeler - Dolgencorp, LLC (068331990)