Dosage & Administration
Helps prevent sunburn.
If used as directed with other sun protection measures, decreases
the risk of skin cancer and early skin aging caused by the sun.
Unme Soulma Centella And Beef Tallow Sunscreen Cream
FDA Label NDC 87472-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Jufeng Qiyuan Trading Co., Ltd. for the product Unme Soulma Centella And Beef Tallow Sunscreen (NDC 87472-001). 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 dosage & administration, warnings, otc - active ingredient, otc - keep out of reach of children, otc - purpose, 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
Warnings
For external use only.
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.
Keep out of reach of children. If swallowed, get medical help
or contact a Poison Control Center right away
Otc - Active Ingredient
Ethylhexyl Methoxycinnamate (Octinoxate) 6.5% - Sunscreen
Octocrylene 6% - Sunscreen
Zinc Oxide 5.59% - Sunscreen
Phenylbenzimidazole Sulfonic Acid (Ensulizole) 2% - Sunscreen
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
Otc - Purpose
Sunscreen
Inactive Ingredient
CI 77891 (Titanium Dioxide), Niacinamide, Panthenol, Tallow,
Dipotassium Glycyrrhizate, Centella Asiatica Extract
Indications & Usage
Apply liberally 15 minutes before sun exposure.
Reapply at least every 2 hours.
Children under 6 months of age: ask a doctor.
Package Label.Principal Display Panel
33 (33)
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