Otc - Active Ingredient
Zinc Oxide 8%Purpose Sunscreen
Wildara Mineral Tallow Sunscreen Spf 50 Cream
FDA Label NDC 87761-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Moes Group Llc for the product Wildara Mineral Tallow Sunscreen Spf 50 (NDC 87761-005). 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, otc - keep out of reach of children, otc - purpose, warnings, dosage & administration, inactive ingredient, indications & usage, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a PoisonControl Center right away
Otc - Purpose
Uses. helps prevent sunburn
Warnings
For external use only
Dosage & Administration
shake well prior to use
apply liberally 15 minutes before sun exposure
Inactive Ingredient
100% Grass-Fed Beef Tallow.Organic Jojoba OIl, OrganicBeeswax, Vanila planifolia(Vanilla) oi, Tocopherol(Vitamin E)
Indications & Usage
Directions shake well prior to useapply lberally 15 minutes before sun exposure .children under 6 months of age: Ask a doctorreapply:.after 80 minutes of swimming or sweating
Package Label.Principal Display Panel
Labeling (87761 005 01)
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