Doterra Sun Face Daily Moisturizer Lotion
FDA Label NDC 71630-147

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Doterra International, Llc for the product Doterra Sun Face Daily Moisturizer (NDC 71630-147). 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, mineral sunscreen daily moisturizer, indications & usage, warnings, otc - when using, other safety information, inactive ingredient, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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