Label: ITCH RELIEF- diphenhydramine hydrochloride, zinc acetate cream
- NDC Code(s): 37808-622-64
- Packager: H E B
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 13, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
Do not use
- •
- on large areas of the body
- •
- with any other product containing diphenhydramine, even one taken by mouth
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
Compare to active ingredients in Extra Strength Benadryl® Cream
Extra Strength
H-E-B®
Itch Relief Cream
2% DIPHENHYDRAMINE HCl and 0.1% ZINC ACETATE
Topical Analgesic & Skin Protectant
Temporary Relief of Itch and Pain due to:
• Insect Bites • Minor Skin Irritations • Rashes from Poison Ivy, Poison Oak or Poison Sumac
NET WT. 1 OZ (28g)
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INGREDIENTS AND APPEARANCE
ITCH RELIEF
diphenhydramine hydrochloride, zinc acetate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-622 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-622-64 1 in 1 CARTON 09/15/2010 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 09/15/2010 Labeler - H E B (007924756)