Label: ITCH STOPPING CREAM- diphenhydramine hydrochloride 2%, zinc acetate 0.1% cream
- NDC Code(s): 69396-150-01
- Packager: Trifecta Pharmaceuticals USA, LLC.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 12, 2024
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- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- INDICATIONS & USAGE
- Warnings
- Do Not Use
- When Using this product
- Stop Use and Ask a Doctor If
- Keep out of the reach of children
- Ask a Doctor before Use
- Directions
- Other information
- Inactive Ingredients
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Distributed By:
Proudly Distributed by Associated Wholesale Grocers Inc.
Kansas City, KS. 66106 USA
Questions Call: 1-877-753-3935
Monday-Friday 9AM-5PM EST
This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., owner of the registered trademark Extra Strength Benadryl® Itch Stopping Cream.
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- Packaging
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INGREDIENTS AND APPEARANCE
ITCH STOPPING CREAM
diphenhydramine hydrochloride 2%, zinc acetate 0.1% creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69396-150 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 2 g in 100 g ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE 0.1 g in 100 g Inactive Ingredients Ingredient Name Strength LAURETH-23 (UNII: N72LMW566G) WATER (UNII: 059QF0KO0R) PETROLATUM (UNII: 4T6H12BN9U) MINERAL OIL (UNII: T5L8T28FGP) CETYL ALCOHOL (UNII: 936JST6JCN) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) STEARIC ACID (UNII: 4ELV7Z65AP) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PROPYLPARABEN (UNII: Z8IX2SC1OH) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69396-150-01 1 in 1 BOX 11/29/2023 1 28.3 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 11/29/2023 Labeler - Trifecta Pharmaceuticals USA, LLC. (079424163)