Label: EXTRA STRENGTH ITCH RELIEF- diphenhydramine hcl and zinc acetate spray
- NDC Code(s): 83324-302-27
- Packager: Chain Drug Marketing Association Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Active ingredients
- Purpose
- Uses
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Warnings
For external use only.
Flammable:
Keep away from fire or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120ºF. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
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?
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INGREDIENTS AND APPEARANCE
EXTRA STRENGTH ITCH RELIEF
diphenhydramine hcl and zinc acetate sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83324-302 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 20 mg in 1 g ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 1 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ALCOHOL (UNII: 3K9958V90M) TROMETHAMINE (UNII: 023C2WHX2V) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83324-302-27 76 g in 1 CAN; Type 0: Not a Combination Product 06/06/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 06/06/2024 Labeler - Chain Drug Marketing Association Inc (011920774)