Purpose
Sunscreen
Sun Serum Drops Liquid
FDA Label NDC 54136-371
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Better Planet Brands Llc for the product Sun Serum Drops (NDC 54136-371). 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 purpose, uses, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
• helps prevent sunburn
Warnings
• For external use
Otc - Do Not Use
• Do not use on damaged or broken skin.
Otc - Stop Use
• Stop use and ask a doctor if rash occurs.
Otc - Keep Out Of Reach Of Children
• Keep out of reach of children.
If product is swallowed get medical help or contact a Poison Control Center right away.
Other Information
• Protect this product from excessive heat and direct sun. • May stain some
Inactive Ingredients
DICAPRYLYL CARBONATE, CAPRYLIC/CAPRIC TRIGLYCERIDE, BUTYLOCTYL SALICYCLATE, TRIDECTYL SALICYCLATE, COCO-CAPRYLATE/ CAPRATE, COCONUT ALKANES, SORBITAN SESQUIOLEATE, POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE, BUTYROSPERMUM PARKII (SHEA) BUTTER*, CETYL ALCOHOL, STEARYL ALCOHOL,
TOCOPHERYL ACETATE (VITAMIN E), CALENDULA OFFICINALIS (POT MARIGOLD) FLOWER, OLEA EUROPEA (OLIVE) FRUIT OIL, LECITHIN, ETHYLHEXYGLYCERIN.
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