Active Ingredient Listing
Active Ingredients: Zinc Oxide12%. Purpose: Sunscreen
White And Elm Everyday Spf 15
FDA Label NDC 70840-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by White & Elm Llc for the product White And Elm Everyday Spf 15 (NDC 70840-001). 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 ingredient listing, otc - ask doctor, inactive ingredient, warnings, otc - do not use, otc - keep out of reach of children, 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 - Ask Doctor
Children under 6 months of age: Ask a doctor.
Inactive Ingredient
Inactive Ingredients: Aloe Barbadensis (Aloe Vera) Leaf Juice, Helianthus Annuus (Sunflower) Seed Oil, Glycerin (Vegetable), Cetearyl Olivate, Benzyl Alcohol, Sorbitan Olivate, Tocopherols (Vitamin E), Xanthan Gum, Dehydroacetic Acid
Warnings
Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs.
Otc - Do Not Use
Do not use on damaged or broken skin.
Otc - Keep Out Of Reach Of Children
Keep out of children’s reach.
Package Label.Principal Display Panel
Mineral Sunscreen
Broad Spectrum SPF 15
* Please review the disclaimer below.
