Supergoop Glow Screen Spf 40 Cream
FDA Label NDC 75936-601

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Supergoop Llc for the product Supergoop Glow Screen Spf 40 (NDC 75936-601). 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, keep out of reach of children, indications and usage, warnings, dosage and administration, inactive ingrediens, package label/pdp, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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