Otc - Active Ingredient
Non-Nano Zinc Oxide 20%
Sunscreen
Lasso Tallow Sunscreen Spf 50 Cream
FDA Label NDC 87761-004
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 Lasso Tallow Sunscreen Spf 50 (NDC 87761-004). 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 - purpose, otc - keep out of reach of children, 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 - Purpose
Helps prevent sunburn
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Warnings
WARNINGS
For external use onlyDo not use on damaged or broken skinWhen using this product keep out of eyes.Rinse with water to remove from eyes.
Dosage & Administration
DIRECTIONS
Apply liberally 15 minutes before sun exposureReapply after 80 minutes of swimming or sweatingImmediately after towel dryingAtleast every 2hours
Inactive Ingredient
Grass-Fed Beef Tallow, Organic Beeswax, Organic Jojoba Oil, Tocopherol
(Vitamin E), Vanilla Planifolia (Vanilla) Oil.
Indications & Usage
Spending time in the sun increases your risk of skin cancer and early skin aging.
To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value
of 15 or higher and other sun protection measures including:Limit time in the sun, especially from 10 a.m. -2 p.m.
Wear long-sleeved shirts, pants, hats, and sunglasses
Package Label.Principal Display Panel
Labeling (87761 004 01)
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