Label: BLUE LIZARD KIDS SPF 50- zinc oxide spray
- NDC Code(s): 0316-2081-05, 0316-2081-45
- Packager: Crown Laboratories
- Category: HUMAN OTC DRUG LABEL
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
Aphanizomenon Flosaquae Extract, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Caprylyl Glycol, Cetyl Diglyceryl Tris(Trimethylsiloxy)silylethyl Dimethicone, Dimethicone, Ethylhexylglycerin, Glycerin, Hydrogen Dimethicone, Hydrogenated Polydecene, Isopropyl Myristate, Pentylene Glycol, Polyhydroxystearic Acid, Potassium Sorbate, Propanediol, Silica, Sodium Benzoate, Sodium Chloride, Sodium Phytate, Sorbitan Olivate, Synthetic Beeswax, Tetrafluoropropene, Water
- Questions?
- Blue Lizard Kids SPF 50+ Spray 5 oz Label
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INGREDIENTS AND APPEARANCE
BLUE LIZARD KIDS SPF 50
zinc oxide sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0316-2081 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 CAPRYLYL GLYCOL (UNII: 00YIU5438U) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) CETYL DIGLYCERYL TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE (3500 MM2/S) (UNII: KB7T6C99UP) 1,3,3,3-TETRAFLUOROPROPENE, (1E)- (UNII: 5I2481UOO8) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) SORBITAN OLIVATE (UNII: MDL271E3GR) GLYCERIN (UNII: PDC6A3C0OX) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N) HYDROGENATED POLY(C6-14 OLEFIN; 4 CST) (UNII: 7C6HV4SSLA) PROPANEDIOL (UNII: 5965N8W85T) PHYTATE SODIUM (UNII: 88496G1ERL) SYNTHETIC BEESWAX (UNII: 08MNR5YE2R) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) DIMETHICONE (UNII: 92RU3N3Y1O) PENTYLENE GLYCOL (UNII: 50C1307PZG) APHANIZOMENON FLOSAQUAE (UNII: 49VG1X560X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0316-2081-05 142 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/29/2021 2 NDC:0316-2081-45 127.6 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)
