NDC | 43617-3417-3 |
Set ID | 1f41955b-a363-495c-91ef-2206efad07fe |
Category | HUMAN OTC DRUG LABEL |
Packager | Lanocorp Pacific Ltd |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
-
DIRECTIONS
Apply liberally and evenly 15 minutes before sun exposure
Children under 6 months of age: Ask a doctor
Apply to all skin exposed to the sun
Reapply at least every 2 hours
Use a water resistant sunscreen if swimming or sweating
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 10am-2pm.
- wear long-sleeved shirts, pants, hats and sunglasses. - OTHER INFORMATION
-
INACTIVE INGREDIENTS
Aqua (water)
Stearic Acid
Persea Gratissima (Avocado) Oil
Simmondsia Chinensis (Jojoba) Oil
Butyloctyl salicylate
Acetylated Lanolin Alcohol
Leptospermum Scoparium Mel
Actinidia Chinensis (Kiwi) Fruit Extract
Hydrolyzed (Marine) Collagen
Tocopheryl Acetate (Vitamin E)
Carbomer
Cetyl Alcohol
Triethanolamine
Caprylhydroxamic Acid
Phenoxiethanol
Methylpropanediol
Tetrasodium EDTA - PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BY NATURE DAILY FACE SUNSCREEN BROAD SPECTRUM SPF 30
octinoxate, titanium dioxide, oxybenzone, avobenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43617-3417 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 g in 1 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 50 g in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 45 g in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 25 g in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) STEARIC ACID (UNII: 4ELV7Z65AP) AVOCADO OIL (UNII: 6VNO72PFC1) JOJOBA OIL (UNII: 724GKU717M) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P) HONEY (UNII: Y9H1V576FH) KIWI FRUIT (UNII: 71ES77LGJC) HYDROLYSED MARINE COLLAGEN (ENZYMATIC; 2000 MW) (UNII: 2WID9OCG7P) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC) CETYL ALCOHOL (UNII: 936JST6JCN) TROLAMINE (UNII: 9O3K93S3TK) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYLPROPANEDIOL (UNII: N8F53B3R4R) EDETATE SODIUM (UNII: MP1J8420LU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43617-3417-3 1 in 1 BOX 1 60 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 02/01/2014 Labeler - Lanocorp Pacific Ltd (594482114) Establishment Name Address ID/FEI Business Operations Lanocorp Pacific Ltd 594482114 manufacture(43617-3417)