Label: ITCH RELIEF- diphenhydramine hcl, zinc acetate spray
- NDC Code(s): 59450-295-20
- Packager: The Kroger Co
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 18, 2024
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- Active ingredients
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- Uses
- Warnings
- Do not use
- Ask a doctor before use
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- Stop use and ask a doctor if
- Keep out of reach of children.
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NDC 59450-295-20
COMPARE TO the active ingredients in BENADRYL ® EXTRA STRENGTH TOPCICAL ANALGESIC SPRAY*
Kroger ®
Extra Strength
Itch Relief Spray
Diphenhydramine HCI 2%
Topcail Analgesic
Zinc Acetone 0.1%
Skin Protectant
Relieves pain and itching due to insect bites, poison ivy or oak, or other minor skin irritations
2 FL OZ (59 mL)
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INGREDIENTS AND APPEARANCE
ITCH RELIEF
diphenhydramine hcl, zinc acetate sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59450-295 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE 1 mg in 1 mL DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) POVIDONE (UNII: FZ989GH94E) TROMETHAMINE (UNII: 023C2WHX2V) ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59450-295-20 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 02/02/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 02/02/2024 Labeler - The Kroger Co (006999528) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(59450-295) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(59450-295)