Otc - Active Ingredient Section
Otc Active Ingredients (Active)
Sunscreen
FDA Label NDC 62932-243
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Private Label Select Ltd Co for the product Sunscreen (NDC 62932-243). 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 otc - active ingredient section, otc - keep out of reach of children, otc - purpose, artwork (back label no. 1), artwork (back label no. 2), artwork (front label), artwork (back label no. 3), and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Otc Purpose (Purpose)
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