Sunscreen
FDA Label NDC 72239-001

The following Structured Product Label (SPL) was submitted to the FDA by Ol Products, Inc. for the product Sunscreen (NDC 72239-001). 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 drug facts acitve ingredients purpose, directions, keep out of reach of children, inactive ingredients, uses, questions, selfie spf 15 - flammable, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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