Active Ingredients Purpose
Niacinamide 0.01%, Vitamin E Acetate 0.50%, Titanium Di Oxide 0.01%, Zinc Oxide 0.01% ................. Sun protection
Mineral Sunscreen Spf 50
FDA Label NDC 83325-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Volans Epic Llc for the product Mineral Sunscreen Spf 50 (NDC 83325-008). 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, use, warnings, when using this product, directions, other lnformation, inactive lngredlents, questions or comments?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Use
For Sun protection
Warnings
FOR EXTERNAL USEONLY.
When Using This Product
■ Avoid contact with eyes. If contact occurs, flush thoroughly with water
Directions
Apply sunscreen evenly, 15 minutes before stepping out.
Other Lnformation
Store in a cool & dry place. Keep away from direct sunlight.
Inactive Lngredlents
Aqua, Octocrylene, Methylene Bis-Benzotriazolyl Tetramethylbutylphenol (and) Aqua (and) Decyl Glucoslde (and) Propylene Glycol (and) Xanthan Gum, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Ethylhexyl Salicylate, Cetyl Alcohol, PEG 100 Stearate & Glyceryl Stearate, C12-15 Alkyl Benzoate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Glycerin, Phenoxyethanol, Fragrance.
Questions Or Comments?
For any customer feedback or queries, write to us at: [email protected] or call us on +1 530-464-6426
Principal Display Panel
Image Description (Mineral Sunscreen Spf 50)
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