Label: CVS ANTI ITCH- hydrocortisone cream
- NDC Code(s): 69842-292-01
- Packager: CVS
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 May 7, 2019
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
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Uses
for the temporary relief of itching associated with minor skin irritations, inflammation, and rashes due to:
eczema
seborrheic dermatitis
psoriasis
insect bites
poison ivy, poison oak, and poison sumac
cosmetics
jewelry
detergents
soaps
temporarily relieves external anal and genital itching
other uses of this product should be only under the advice and supervision of a doctor
- Warnings
- Directions
- Other information
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Inactive ingredient
aloe barbadensis (aloe vera) leaf juice, anhydrous citric acid, avena sativa (oat) kernel extract, avena sativa (oat) kernel flour, avena sativa (oat) kernel oil, benzyl alcohol, ceteareth-20, cetostearyl alcohol, cetyl palmitate, cyclopentasiloxane, dimethicone/vinyltrimethylsiloxysilicate, glycerin, isopropyl myristate, isostearyl neopentanoate, methylparaben,
polyoxyl 40 stearate, potassium lactate, purified water, sodium hydroxide, vitamin E - Purpose
- Content of labeling
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INGREDIENTS AND APPEARANCE
CVS ANTI ITCH
hydrocortisone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-292 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 CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) METHYLPARABEN (UNII: A2I8C7HI9T) WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) POTASSIUM LACTATE (UNII: 87V1KMK4QV) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) VINYLTRIMETHYLSILYLOXY SILICATE (UNII: XZ65AY5QAK) SODIUM HYDROXIDE (UNII: 55X04QC32I) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) PEG-40 STEARATE (UNII: ECU18C66Q7) CETYL PALMITATE (UNII: 5ZA2S6B08X) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) OAT KERNEL OIL (UNII: 3UVP41R77R) DIMETHICONE (UNII: 92RU3N3Y1O) BENZYL ALCOHOL (UNII: LKG8494WBH) ISOSTEARYL NEOPENTANOATE (UNII: 411THY156Q) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-292-01 1 in 1 CARTON 02/10/2016 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 not final part348 02/10/2013 Labeler - CVS (062312574) Registrant - Weeks & Leo (005290028) Establishment Name Address ID/FEI Business Operations Weeks & Leo Co., Inc. 005290028 manufacture(69842-292)