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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Sknvcare, Llc for the product Sunscreen (NDC 82704-3019). 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 other, active ingredients, purpose, uses, warnings, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Octocrylene 5.0%
Octisalate 3.0%
Avobenzone 2.5%
Sunscreen
For external use only
Flammable:Do not use near heat, flame, or while smoking
Do not useon damaged or broken skin
When using this product:
Stop use and ask a doctorif rash occurs
Keep out of reach of children.If product is swallowed, get medical help or contact a Poison Control Center right away.
alcohol , deionized water, lauryl lactate, cyclopentasiloxane, c12-15 alcohols benzoate, 2-butyloctyl, salicylate octyldodecyl neopentanoate, ethyl cellulose and fragrance.
* Please review the disclaimer below.