Active Ingredients
Diphenhydramine HCL 2%
Zinc acetate 0.1%
The following Structured Product Label (SPL) was submitted to the FDA by Old East Main Co. for the product Itch Relief (NDC 55910-295). 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 external use only
on chicken pox or measles
do not get in eyes
condition worses 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.
store at 20⁰ to 25⁰ C (68⁰ to 77⁰ F)
alcohol, glycerin, povidone, purified water, tris (hydroxymethyl) aminomethane
*Not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Benadryl Spray
DISTRIBUTED BY DOLGENCORP, LLC
100 MISSION RIDE
GOODLETTSVILLE, TTN 37072
* Please review the disclaimer below.