Label: CORTIZONE 10 ANTI-ITCH FOR DIABETICS SKIN- hydrocortisone lotion
- NDC Code(s): 41167-0342-0
- Packager: Chattem, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 25, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
When using this product
- avoid contact with eyes
- do not use more than directed unless told to do so by a doctor
- avoid contact with eyes
- Directions
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Inactive ingredients
water, glycerin, dimethicone, petrolatum, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, cetyl alcohol, dextrin, glyceryl stearate, ishexadecane, methyl gluceth-20, aloe barbadensis leaf extract, avena sativa (oat) kernel extract, chamomilla recutita (matricaria) flower extract, butyrospermum parkii (shae) butter extract, boswellia serrata gum, zingiber officinale (ginger) root extract, bisabolol, magnesium ascorbyl phosphate, tocopheryl acetate, malodextrin, ethylhexylglycerin, dehydroacetic acid, polysorbate 60, phenoxyethanol, disodium EDTA, dipropylene glycol, benzoic acid, pentylene glycol, 4-t-butylcyclohexanol, sodium citrate
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INGREDIENTS AND APPEARANCE
CORTIZONE 10 ANTI-ITCH FOR DIABETICS SKIN
hydrocortisone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41167-0342 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 WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) PETROLATUM (UNII: 4T6H12BN9U) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) CETYL ALCOHOL (UNII: 936JST6JCN) ICODEXTRIN (UNII: 2NX48Z0A9G) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ISOHEXADECANE (UNII: 918X1OUF1E) METHYL GLUCETH-20 (UNII: J3QD0LD11P) ALOE VERA LEAF (UNII: ZY81Z83H0X) OAT (UNII: Z6J799EAJK) CHAMOMILE (UNII: FGL3685T2X) SHEANUT OIL (UNII: O88E196QRF) INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) GINGER (UNII: C5529G5JPQ) LEVOMENOL (UNII: 24WE03BX2T) MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) MALTODEXTRIN (UNII: 7CVR7L4A2D) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) DEHYDROACETIC ACID (UNII: 2KAG279R6R) POLYSORBATE 60 (UNII: CAL22UVI4M) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) DIPROPYLENE GLYCOL (UNII: E107L85C40) BENZOIC ACID (UNII: 8SKN0B0MIM) PENTYLENE GLYCOL (UNII: 50C1307PZG) 4-TERT-BUTYLCYCLOHEXANOL (UNII: K0H1405S9C) SODIUM CITRATE (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41167-0342-0 1 in 1 CARTON 12/22/2014 1 96 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 12/22/2014 Labeler - Chattem, Inc. (003336013)