Active Ingredients
Diphenhydramine HCl 2%
Zinc Acetate 0.1%
The following Structured Product Label (SPL) was submitted to the FDA by Retail Business Services, Llc for the product Itch Relief (NDC 72476-295). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, do not use, ask a doctor before use, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Diphenhydramine HCl 2%
Zinc Acetate 0.1%
External analgesic
Skin protectant
•for the temporary relief of pain and itching associated with minor skin irritations
•dries the oozing and weeping of poison: iv, oak, sumac
For external use only
Flammable. Keep away from fire of flame.
•on large areas of the body •with any other product containing diphenhydramine, even one taken by mouth
on chicken pox or measles
do not get into eyes
condition worsens or symptoms last more than 7 days or clear up and occur again within a few days
If swallowed, get medical help or contact a Poison Control Center right away.
•do 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
• store at 20⁰ - 25⁰C (68⁰ - 77⁰F)
alcohol, glycerin, povidone, purified water, tris (hydroxymethyl)aminomethane
Not manufactured or distributed by Johnson + Johnson Consumer Products Company, distributor of Benadryl Spray*
DIST. BY FOODHOLD U.S.A., LLC
LANDOVER, MD 20785
1-877-846-9949 Ahold Delhaize Licensing Sari
Quilty guaranteed or money back
* Please review the disclaimer below.