NDC | 51346-038-01 |
Set ID | 02b9558d-53ac-4f05-aafa-045a04ad82a1 |
Category | HUMAN OTC DRUG LABEL |
Packager | NATURE REPUBLIC CO., LTD. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive Ingredients:
WATER, CYCLOPENTASILOXANE, GLYCERIN, DIPROPYLENE GLYCOL, PEG-10 DIMETHICONE, DIMETHICONE, TALC, DISTEARDIMONIUM HECTORITE, ISODECYL NEOPENTANOATE, OCTYLDODECYL NEOPENTANOATE, MAGNESIUM SULFATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, PHENOXYETHANOL, METHYL METHACRYLATE CROSSPOLYMER, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, METHICONE, FRAGRANCE, METHYLPARABEN, POLYGLYCERYL-6 POLYRICINOLEATE, PROPYLPARABEN, SEA WATER, TRIHYDROXYSTEARIN,
IRON OXIDES, ALOE BARBADENSIS LEAF JUICE, CENTELLA ASIATICA EXTRACT, HAMAMELIS VIRGINIANA (WITCH HAZEL) BARK/LEAF/TWIG EXTRACT, HEDERA HELIX (IVY) EXTRACT, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, MACADAMIA TERNIFOLIA SEED OIL, BUTYLPARABEN - PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS AND USAGE
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL. PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
UV LOCK FLOWER DAILY POWERFUL SUN SPF50PLUS PA PLUS PLUS PLUS
octinoxate, octisalate, zinc oxide, titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51346-038 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 3.75 g in 50 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 2.50 g in 50 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 2.40 g in 50 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 1.25 g in 50 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) GLYCERIN (UNII: PDC6A3C0OX) DIPROPYLENE GLYCOL (UNII: E107L85C40) DIMETHICONE (UNII: 92RU3N3Y1O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51346-038-01 50 mL in 1 CARTON Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 01/02/2012 Labeler - NATURE REPUBLIC CO., LTD. (631172020) Registrant - NATURE REPUBLIC CO., LTD. (631172020) Establishment Name Address ID/FEI Business Operations NATURE REPUBLIC CO., LTD. 631172020 manufacture(51346-038)