Sunscreen
FDA Label NDC 62932-217

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 62932-217). 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 dosage and administration, warnings section, inactive ingredients, indications and usage, otc keep put of reach of children, otc active ingredient, otc purpose, label/artwork, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.