Active Ingredients Purpose
Diphenhydramine HCl – 2% Topical analgesic
Zinc Acetate – 0.1% Skin Protectant
Itch Rel Spr
FDA Label NDC 69842-845
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cvs for the product Itch Rel Spr (NDC 69842-845). 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, ask a doctor before use, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
temporarily relieves itching and pain associated with minor irritations, burns, scrapes, cuts, insect bites and rashes due to poison oak & poison sumac. Dries the oozing and weeping of poison ivy, poison oak & poison sumac.
Ask A Doctor Before Use
• on chicken pox
• on measles
Directions
• 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
Other Information
Store at 20 o - 25 oC (68 o - 77 oF)
Inactive Ingredients
Alcohol, Glycerin, Povidone, Purified Water, Tromethamine
* Please review the disclaimer below.
