Label: DUKE CANNON STANDARD ISSUE FACE- sunscreen lotion
- NDC Code(s): 60717-906-17
- Packager: RNA PHARMA, LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated September 21, 2021
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INGREDIENTS AND APPEARANCE
DUKE CANNON STANDARD ISSUE FACE
sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60717-906 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 0.05 g in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 0.03 g in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 0.065 g in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 0.02 g in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 0.075 g in 1 mL Inactive Ingredients Ingredient Name Strength XANTHAN GUM (UNII: TTV12P4NEE) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETEARYL OLIVATE (UNII: 58B69Q84JO) EDETATE DISODIUM (UNII: 7FLD91C86K) ETHYLHEXYL PALMITATE (UNII: 2865993309) AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) RICE BRAN (UNII: R60QEP13IC) ROSEMARY (UNII: IJ67X351P9) TOCOPHEROL (UNII: R0ZB2556P8) CAPRYLYL GLYCOL (UNII: 00YIU5438U) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) GLYCERYL 1-STEARATE (UNII: 258491E1RZ) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) SORBITAN OLIVATE (UNII: MDL271E3GR) EICOSYL POVIDONE (UNII: XQQ9MKE2BJ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60717-906-17 50 mL in 1 TUBE; Type 0: Not a Combination Product 09/21/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 09/21/2021 Labeler - RNA PHARMA, LLC (079103999) Establishment Name Address ID/FEI Business Operations RNA PHARMA, LLC 079103999 manufacture(60717-906)