Label: 2X SUNBLOCK SPF 50- avobenzone, homosalate, octocrylene, oxybenzone liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 76174-120-01 - Packager: Nupur Formulations Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 April 28, 2011
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SPL UNCLASSIFIED SECTION
Dr. Nic Martens - a biochemist and athlete - developed SCAPE Athlete Sunblock to address the protection and performance needs of athletes. The formula's engineered polymers bond to skin for long lasting waterproofing and sweatproofing that won't run into your eyes. SCAPE Athlete Sunblock provides superior UVA + UVB protection in a non-greasy, noncomedogenic formula that allows you to maintain optimal core body temperature and lets your skin breathe naturally.
- DOSAGE & ADMINISTRATION
- WARNINGS
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients:
Water (Aqua), Styrene/Acrylates Copolymer, Butyloctyl Salicylate,Octyldodecyl Neopentanoate, Potassium Cetyl Phosphate, VP/Eicosene Copolymer, Silica,Cyclopentasiloxane, Trimethylsiloxysilicate, Tocopherol, Dipotassium Glycyrrhizate, Stearic Acid, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Disodium EDTA, Caprylyl Glycol, Phenoxyethanol, Methylparaben, Propylparaben, Fragrance (Parfum)
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
2X SUNBLOCK SPF 50
avobenzone, homosalate, octocrylene, oxybenzone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76174-120 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 mL in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 15 mL in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 6 mL in 100 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 6 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) STEARIC ACID (UNII: 4ELV7Z65AP) C10-30 CHOLESTEROL/LANOSTEROL ESTERS (UNII: 137SL7IL0Y) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) EDETATE DISODIUM (UNII: 7FLD91C86K) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76174-120-01 37 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/22/2011 Labeler - Nupur Formulations Inc (246855006)
