Uses
Temporarily relieves pain and itching due to: • sunburn • minor burns • minor cuts • scrapes • insect bites • minor skin irritations
Medicated Pain Relief Foot
FDA Label NDC 11822-7799
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rite Aid for the product Medicated Pain Relief Foot (NDC 11822-7799). 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
Alcohol Denat.
Aloe Barbadensis Leaf Extract
Carbomer
Chamomilla Recutita (Matricaria) Flower Extract
Cucumis Sativus (Cucumber) Fruit Extract
Diazolidinyl Urea
Disodium Cocoamphodipropionate
Disodium EDTA
Glycerin
Propylene Glycol
Simethicone
Tocopheryl Acetate
Triethanolamine
Water
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