Label: CORTIZONE 10 FEMININE ITCH RELIEF- hydrocortisone cream
- NDC Code(s): 41167-0330-3
- Packager: Chattem, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 26, 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
Do not use
■ for the treatment of diaper rash. Consult a doctor. ■ if you have vaginal discharge. Consult a doctor. ■ if you are allergic to any ingredient in this product
When using this product
■ avoid contact with eyes ■ do not use more than directed unless told to do so by a doctor
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Directions
■ when practical, clean the affected area with mild soap and warm water and rinse thoroughly then gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product
■ adults and children 12 years of age and older: apply a fingertip amount (approximately 1-inch strip) to affected area not more than 3 to 4 times daily
■ children under 12 years of age: ask a doctor
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Inactive ingredients
water, glycerin, dimethicone, petrolatum, jojoba esters, cetyl alcohol, aloe barbadensis leaf juice, stearyl alcohol, distearyldimonium chloride, cetearyl alcohol, steareth-2, steareth-21, chamomilla recutita (matricaria) flower extract, tocopheryl acetate, magnesium ascorbyl phosphate, retinyl palmitate, hydrolyzed jojoba esters, beta-glucan, glyceryl stearate, menthyl lactate, polysorbate 60, methyl gluceth-20, stearamidopropyl PG-dimonium chloride phosphate, PPG-12/SMDI copolymer, potassium hydroxide, diazolidinyl urea, propylene glycol, benzyl alcohol, methylparaben, BHT, propylparaben, EDTA
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CORTIZONE 10 FEMININE ITCH RELIEF
hydrocortisone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41167-0330 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) JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL) CETYL ALCOHOL (UNII: 936JST6JCN) ALOE VERA LEAF (UNII: ZY81Z83H0X) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) STEARETH-2 (UNII: V56DFE46J5) STEARETH-21 (UNII: 53J3F32P58) CHAMOMILE (UNII: FGL3685T2X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W) TRANSFORMING GROWTH FACTOR BETA RECEPTOR TYPE 3 (UNII: 18YWT2KYS8) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) POLYSORBATE 60 (UNII: CAL22UVI4M) METHYL GLUCETH-20 (UNII: J3QD0LD11P) STEARAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: W6000VEI5Y) PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BENZYL ALCOHOL (UNII: LKG8494WBH) METHYLPARABEN (UNII: A2I8C7HI9T) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) PROPYLPARABEN (UNII: Z8IX2SC1OH) EDETIC ACID (UNII: 9G34HU7RV0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41167-0330-3 1 in 1 CARTON 01/01/2023 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 Drug M017 01/01/2023 Labeler - Chattem, Inc. (003336013)
