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 31, 2025
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- Official Label (Printer Friendly)
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Active ingredientsDiphenhydramine HCl 2% Zinc acetate 0.1%
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PurposeExternal analgesic - Skin protectant
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Usesfor the temporary relief of pain and itching associated with minor skin irritations - dries the oozing and weeping of poison: ivy, oak and sumac
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WarningsFor external use only - Flammable. Keep away from fire or flame.
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Do not useon large areas of the body - with any other product containing diphenhydramine, even one taken by mouth
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Ask a doctor before useon chicken pox or measles
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When using this productdo not get into eyes
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Stop use and ask a doctor ifcondition worsens or symptoms last more than 7 days or clear up and occur again within a few days.
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Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.
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Directionsdo not use more than directed - adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily - children under 2 years of age: ask a doctor
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Otherstore at 20º to 25º C (68º to 70ºF)
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Inactive ingredientsalcohol, glycerin, povidone, purified water, tris (hydroxymethyl) aminomethane
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Questions?1-800-632-6900
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Adverse reactionDISTRIBUTED BY THE KROGER CO.CINCINNATI, OHIO 45202
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DisclaimerBenadryl - ®is a registered trademark of Kenvue, Inc. Kenvue, Inc. is not affiliated with The Kroger Co. or this product.
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Principal display panelTEAR HERE - NDC 59450-295-20 - COMPARE TO the active ingredients in BENADRYL - ®EXTRA STRENGTH TOPCICAL ANALGESIC SPRAY* Kroger - ® Extra Strength - Itch Relief Spray - Diphenhydramine HCI ...
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INGREDIENTS AND APPEARANCEProduct Information