Uses
Temporarily relieves pain and itching due to: • sunburn • minor burns • minor cuts • scrapes • insect bites • minor skin irritations
Pain Relief
FDA Label NDC 69842-049
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 Pain Relief (NDC 69842-049). 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 uses, warningsfor external use only., inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warningsfor External Use Only.
Flammable: Do not use while smoking or near heat or flame Do not use in large quantities, particularly over raw surfaces or blistered areas
When using this product
• keep out of eyes
• use only as directed.
• do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.
Stop use and ask doctor if
• condition gets worse • symptoms last more than 7 days
• symptoms clear up and occur again in a few days
Inactive Ingredients
Aloe Barbadensis Leaf Juice, SD Alcohol 40, Propylene Glycol, Glycerin,
Simethicone, Tocopheryl Acetate, Triethanolamine, Carbomer,
Diazolidinyl Urea, Methylparaben, Propylparaben, Disodium
Cocoamphodipropionate, Disodium EDTA
* Please review the disclaimer below.
