Label: SUNLIGHT DAILY FACIAL SPF 30- sunscreen lotion
- NDC Code(s): 76150-293-34
- Packager: Bell International Laboratories, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 6, 2023
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- Active Ingredient
- Uses
- Warnings
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Directions
Apply liberally 15 minutes before sun exposure. Children under 6 months of age: ask a doctor. Reapply at least every 2 hours. Reapply after swimming or sweating. Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrase this risk, regularly use a sunscreen with a Broad Spectrum value of 15 or higher and other sun protection measures including:
- Limit time in the sun, especially from 10 a.m. to 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses
- Use a water resistant sunscreen if swimming or sweating.
- Other Informaiton
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Inactive Ingredients
Bisabolol, Butyloctyl Salicylate, Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, Cetearyl Olivate, Cetyl Palmitate, Citric Acid, Coco-Caprylate/Caprate, Coconut Alkanes, Ethyl Ferulate, Ethylhexyl Olivate, Glyceryl Caprylate, Glyceryl Undecylenate, Heptyl Undecylenate, Phenothyl Alcohol. Polyhydroxstearic Acid, Propanediol, Sodium Hyaluronate, Sodium Phytate, Sodium Stearoyl Glutamate, Sorbitan Oleate, Sorbitan Olivate, Sorbitan Palmitate, Squalene, Tocopherol, Triethoxycaprylylsilane, Vitis Vinifera (Grape) Seed Oil, Water, Xanthan Gum
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INGREDIENTS AND APPEARANCE
SUNLIGHT DAILY FACIAL SPF 30
sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76150-293 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 12.5 g in 100 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) XANTHAN GUM (UNII: TTV12P4NEE) TOCOPHEROL (UNII: R0ZB2556P8) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544) HYALURONATE SODIUM (UNII: YSE9PPT4TH) ETHYL FERULATE (UNII: 5B8915UELW) CETEARYL OLIVATE (UNII: 58B69Q84JO) COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) WATER (UNII: 059QF0KO0R) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) LEVOMENOL (UNII: 24WE03BX2T) PHYTATE SODIUM (UNII: 88496G1ERL) HEPTYL UNDECYLENATE (UNII: W77QUB6GXO) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) PROPANEDIOL (UNII: 5965N8W85T) SQUALANE (UNII: GW89575KF9) SORBITAN MONOPALMITATE (UNII: 77K6Z421KU) COCONUT ALKANES (UNII: 1E5KJY107T) CETYL PALMITATE (UNII: 5ZA2S6B08X) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) GRAPE SEED OIL (UNII: 930MLC8XGG) ETHYLHEXYL OLEATE (UNII: R34927QY59) SHEA BUTTER (UNII: K49155WL9Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76150-293-34 30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/14/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 04/14/2021 Labeler - Bell International Laboratories, Inc (967781555)
