Label: CLEAR CHOISE SUNSCREEN BROAD SPECTRUM SPF 30 WATER RESISTANT COVER SHIELD- zinc oxide lotion
- NDC Code(s): 83722-002-00
- Packager: Dermastart Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 7, 2024
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- Drug Facts
- Active Ingredient
- Uses
- Warnings
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Directions
- apply liberally 15 minutes before sun exposure
- reapply
- after 80 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
- Sun Protection Measures.Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m.-2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses
- children under 6 months of age: Ask a doctor
- Other information
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Inactive ingredients
Caprylic/Capric Triglyceride, Helianthus Annuus (Sunflower) Oil, Squalane Oil (Olive), Dicaprylyl Carbonate, Cetearyl Olivate (and) Sorbitan Olivate, Glycerin, Water (Aqua), Shea Butter Cetyl Esters, Sorbitan Sesquioleate, Polyhydroxystearic Acid,Diglycerin (and) Pinus Pinaster Bark Extract), Punica Granatum (Pomegranate) seed Oil, Phenethyl Alcohol (and) Pentylene Glycol (and) Propanediol, Aloe Barbadensis (Aloe Vera) Leaf Juice, Panthenol, Xanthan Gum, Lauroyl Lysine.
- Label
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INGREDIENTS AND APPEARANCE
CLEAR CHOISE SUNSCREEN BROAD SPECTRUM SPF 30 WATER RESISTANT COVER SHIELD
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83722-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 200 mg in 1 mL Inactive Ingredients Ingredient Name Strength MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) GREEN OLIVE (UNII: 6HD2W46UEG) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) CETEARYL OLIVATE (UNII: 58B69Q84JO) SORBITAN OLIVATE (UNII: MDL271E3GR) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) SHEA BUTTER CETYL ESTERS (UNII: ZRK67KZ6DP) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) DIGLYCERIN (UNII: 3YC120743U) MARITIME PINE (UNII: 50JZ5Z98QY) POMEGRANATE (UNII: 56687D1Z4D) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) PENTYLENE GLYCOL (UNII: 50C1307PZG) PROPANEDIOL (UNII: 5965N8W85T) ALOE VERA LEAF (UNII: ZY81Z83H0X) PANTHENOL (UNII: WV9CM0O67Z) XANTHAN GUM (UNII: TTV12P4NEE) LAUROYL LYSINE (UNII: 113171Q70B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83722-002-00 120 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug OKM020 03/01/2024 Labeler - Dermastart Inc (146909283)
