Label: BLUE LIZARD SPORT SPF 50- zinc oxide spray
- NDC Code(s): 0316-2080-05, 0316-2080-45
- Packager: Crown Laboratories
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 5, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
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Directions
• shake well before and frequently during use
• apply liberally 15 minutes before sun exposure
• hold container 4 to 6 inches from the skin to apply
• do not spray directly into face. Spray on hands then apply to face.
• do not apply in windy conditions.
• use in a well-ventilated area and avoid inhalation
• children under 6 months of age: Ask a doctor
• 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
• reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours
- Other information
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Inactive ingredients
Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Caprylyl Glycol, Cetyl Diglyceryl Tris(Trimethylsiloxy)silylethyl Dimethicone, Copper Gluconate, Dimethicone, Ethylhexylglycerin, Glycerin, Hydrogen Dimethicone, Hydrogenated Polydecene, Isopropyl Myristate, Magnesium Aspartate, Pentylene Glycol, Phenoxyethanol, Polyhydroxystearic Acid, Propanediol, Silica, Sodium Chloride, Sodium Phytate, Sorbitan Olivate, Synthetic Beeswax, Tetrafluoropropene, Water, Zinc Gluconate
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- Blue Lizard Sport SPF 50+ Spray 5 oz Label
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INGREDIENTS AND APPEARANCE
BLUE LIZARD SPORT SPF 50
zinc oxide sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0316-2080 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 24 mg in 1 g Inactive Ingredients Ingredient Name Strength ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) DIMETHICONE (UNII: 92RU3N3Y1O) HYDROGENATED POLY(C6-14 OLEFIN; 4 CST) (UNII: 7C6HV4SSLA) PHYTATE SODIUM (UNII: 88496G1ERL) CETYL DIGLYCERYL TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE (3500 MM2/S) (UNII: KB7T6C99UP) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) MAGNESIUM ASPARTATE (UNII: R17X820ROL) SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) COPPER GLUCONATE (UNII: RV823G6G67) HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N) SYNTHETIC BEESWAX (UNII: 08MNR5YE2R) SORBITAN OLIVATE (UNII: MDL271E3GR) ZINC GLUCONATE (UNII: U6WSN5SQ1Z) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) 1,3,3,3-TETRAFLUOROPROPENE, (1E)- (UNII: 5I2481UOO8) GLYCERIN (UNII: PDC6A3C0OX) PENTYLENE GLYCOL (UNII: 50C1307PZG) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) PROPANEDIOL (UNII: 5965N8W85T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0316-2080-05 142 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/29/2021 2 NDC:0316-2080-45 127.6 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/07/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 03/29/2021 Labeler - Crown Laboratories (079035945) Registrant - Crown Laboratories (079035945)