Active Ingredients
Menthol 0.5%
Walgreens Sunburn Relief Gel
FDA Label NDC 0363-0966
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Company for the product Walgreens Sunburn Relief (NDC 0363-0966). 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, when using this product, stop use and ask a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
External Analgesic
Uses
For the temporary relief of pain and itching associated with sunburn, minor burns, minor cuts, scrapes, insect bites, and minor skin irritations.
Warnings
For External Use Only
When Using This Product
avoid contact with eyes. If contact occurs, rinse with water to remove.
Stop Use And Ask A Doctor If
- condition worsens
- symptoms persist for more than 7 days
- symptoms clear up and occur again within a few days
Keep Out Of Reach Of Children
- If swallowed, seek medical help or contact a Poison Control Center immediately.
Directions
- 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.
Inactive Ingredients:
aloe barbadensis leaf juice, isoceteth-20, triethanolamine, carbomer, allantoin, benzophenone-4, tetrasodium EDTA, propylene glycol, methylparaben, propylparaben, diazolidinyl urea, blue 1, water.
Package Label.Principal Display Panel
W9775a4 (W97754a4)
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