Label: GOOD SENSE ITCH RELIEF- diphenhydramine hydrochloride, zinc acetate cream
- NDC Code(s): 0113-0622-64
- Packager: L. Perrigo Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 24, 2024
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- Active ingredients
- Purpose
- Uses
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Warnings
For external use only
Do not use
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- on large areas of the body
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- with any other product containing diphenhydramine, even one taken by mouth
- Directions
- Other information
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
GOOD SENSE ITCH RELIEF
diphenhydramine hydrochloride, zinc acetate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0113-0622 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 CETYL ALCOHOL (UNII: 936JST6JCN) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) DIETHYLENE GLYCOL MONO- AND DIPALMITOSTEARATE (UNII: 94YQ11Y95F) PEG-20 STEARATE (UNII: NBX892EA57) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0113-0622-64 1 in 1 CARTON 07/18/2006 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 07/18/2006 Labeler - L. Perrigo Company (006013346)