NDC | 51346-213-01 |
Set ID | 5eaa5cb3-b8df-4193-802b-e5d488a5fbc7 |
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:
MICA, TALC, SILICA, NYLON-12, BISMUTH OXYCHLORIDE, MAGNESIUM STEARATE, PHENYL METHICONE, CAPRYLIC/CAPRIC TRIGLYCERIDE, LAUROYL LYSINE, SQUALANE, TRIETHOXYCAPRYLYLSILANE, DIPHENYL DIMETHICONE/VINYL DIPHENYL DIMETHICONE/SILSESQUIOXANE CROSSPOLYMER, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, DIISOSTEARYL MALATE, LANOLIN WAX, IRON OXIDES(CI77492), ALUMINUM MYRISTATE, FRAGRANCE, METHICONE, METHYLPARABEN, ALLANTOIN, TOCOPHERYL ACETATE, IRON OXIDES(CI77491), C9-15 FLUOROALCOHOL PHOSPHATE, PROPYLPARABEN, IRON OXIDES(CI77499), OPUNTIA FICUS-INDICA EXTRACT, PORTULACA OLERACEA EXTRACT, WATER, ARNICA MONTANA FLOWER EXTRACT, CENTAUREA CYANUS FLOWER EXTRACT, DIANTHUS CARYOPHYLLUS FLOWER EXTRACT, FREESIA REFRACTA EXTRACT, IRIS VERSICOLOR EXTRACT, JASMINUM OFFICINALE (JASMINE) FLOWER/LEAF EXTRACT, ZANTEDESCHIA AETHIOPICA FLOWER/STEM EXTRACT, BUTYLENE GLYCOL - PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS AND USAGE
- DOSAGE AND ADMINISTRATION
- PACKAGE LABEL. PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
UV LOCK FLOWER PACT SUN SPF50PLUS PA PLUS PLUS PLUS
titanium dioxide, octinoxate, zinc oxide powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51346-213 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.61 g in 8 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 0.23 g in 8 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 0.24 g in 8 g Inactive Ingredients Ingredient Name Strength MICA (UNII: V8A1AW0880) TALC (UNII: 7SEV7J4R1U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51346-213-01 8 g in 1 CARTON Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 02/01/2013 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(51346-213)