NDC | 75936-215-01, 75936-215-02, 75936-215-03, 75936-215-04, 75936-215-05, 75936-215-06 |
Set ID | 8247aefc-deaa-5333-e053-2991aa0a7e3b |
Category | HUMAN OTC DRUG LABEL |
Packager | Taylor James |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
-
DOSAGE & ADMINISTRATION
Directions
Apply liberally 15 minutes before sun exposure
Reapply:
after 80 minutes of swimming or sweating
immediately after towel drying
at least every 2 hours
Sun Protection Measures. Spending time in the sun increases your risk of skincancer and early skin aging. To decrease this risk, regularly use a sunscreen
with broad spectrum SPF of 15 or higher and other sun protection measures
including:limit time in the sun, especially from 10 a.m. - 2 p.m.
Wear Long-sleeved shirts, pants, hats, and sunglasses
Children under 6 months: Ask a doctor -
INACTIVE INGREDIENT
Inactive Ingredients
Water, Isododecane, Polyester-8, Glycerin, Cetyl Alcohol, Potassium Cetyl Phosphate, Acrylates Copolymer, Oryza Sativa (Rice) Bran Extract, Diisopropyl Sebacate, Isodecyl Neopentanoate, Lauryl Lactate, Cetearyl Olivate, Ammonium Acryloyldimethyltaurate/VP Copolymer, Hydroxyacetophenone, Sorbitan Olivate, Diethylhexyl Syringylidenemalonate, Aniba Roseadora (Rosewood) Wood Oil, Chlorphenesin, Citrus Aurantium Dulcis (Orange) Peel Oil, Citrus Limon (Lemon) Peel Oil, Ethylhexylglycerin, Eucalyptus Globulus Leaf Oil, Ocimum Basilicum (Basil) Flower/leaf Extract, Pelargonium Graveolens Flower Oil, Pogostemon Cablin Oil, 1,2-Hexanediol, Caprylyl Glycol, Xanthan Gum, Helianthus Annuus (Sunflower) Extract, Behenix Acid, Cetyl Behenate, Isostearyl Isostearate, Pentylene Glycol, Trisodium Ethylenediamine Disuccinate, Tocopherol, Allantoin, Rosmarinus Officinalis (Rosemary) Leaf Extract, Caprylic/Capric Triglyceride, Panthenol, Pentasodium Triphosphate, Citric Acid
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
EVERYDAY SUNSCREEN SPF 50 WITH SUNFLOWER EXTRACT
avobenzone, homosalate, octinoxate, octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75936-215 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CETYL ALCOHOL (UNII: 936JST6JCN) ALLANTOIN (UNII: 344S277G0Z) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) PANTHENOL (UNII: WV9CM0O67Z) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) RICE BRAN (UNII: R60QEP13IC) ISODECYL NEOPENTANOATE (UNII: W60VYE24XC) LAURYL LACTATE (UNII: G5SU0BFK7O) CETEARYL OLIVATE (UNII: 58B69Q84JO) SORBITAN OLIVATE (UNII: MDL271E3GR) DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248) CHLORPHENESIN (UNII: I670DAL4SZ) EUCALYPTUS OIL (UNII: 2R04ONI662) PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CETYL BEHENATE (UNII: WFM51TRO3E) ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y) PENTYLENE GLYCOL (UNII: 50C1307PZG) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) TOCOPHEROL (UNII: R0ZB2556P8) SODIUM TRIPOLYPHOSPHATE ANHYDROUS (UNII: 9SW4PFD2FZ) LEMON OIL (UNII: I9GRO824LL) XANTHAN GUM (UNII: TTV12P4NEE) ROSEMARY (UNII: IJ67X351P9) ISODODECANE (UNII: A8289P68Y2) POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) DIISOPROPYL SEBACATE (UNII: J8T3X564IH) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) ROSEWOOD OIL (UNII: F2522O5L7B) ORANGE OIL (UNII: AKN3KSD11B) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PATCHOULI OIL (UNII: F3IN55X5PO) BEHENIC ACID (UNII: H390488X0A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75936-215-01 532 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/19/2019 2 NDC:75936-215-02 222 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/19/2019 3 NDC:75936-215-03 71 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/19/2019 4 NDC:75936-215-04 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/19/2019 5 NDC:75936-215-05 10 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/19/2019 6 NDC:75936-215-06 3 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/19/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/19/2019 Labeler - Taylor James (033381850) Establishment Name Address ID/FEI Business Operations Cosway Company, Inc. 620899877 manufacture(75936-215)