Label: ITCH RELIEF- diphenhydramine hcl and zinc acetate spray
- NDC Code(s): 79903-217-25
- Packager: Wal-Mart Stores, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 August 28, 2023
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- Active ingredients
- Purpose
- Uses
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Warnings
For external use only.
Do not use
- on large areas of the body
- on chicken pox, poison ivy, or sunburn
- on broken, blistered, or oozing skin
- more often than directed
- with any other product containing diphenhydramine, even one taken by mouth
- Directions
- Other information
- Inactive ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
ITCH RELIEF
diphenhydramine hcl and zinc acetate sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-217 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 mL Inactive Ingredients Ingredient Name Strength CAMPHOR (NATURAL) (UNII: N20HL7Q941) POVIDONE (UNII: FZ989GH94E) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) TROMETHAMINE (UNII: 023C2WHX2V) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-217-25 74 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/28/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M017 08/28/2023 Labeler - Wal-Mart Stores, Inc. (051957769)