NDC | 65364-210-59 |
Set ID | 9e23a8ed-3ac4-4b45-95c3-df383468ff26 |
Category | HUMAN OTC DRUG LABEL |
Packager | Kiss My Face LLC |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions
• Apply liberally 15 minutes before sun exposure • Reapply after 40 minutes swimming/sweating • immediately after towel drying • atleast every 2 hours • Children under 6 months: Ask a doctor • Sun Protection Measures Spending time in the sun increases your risk of skin cancer/skin aging. To decrease risk, use Broad Spectrum sunscreen SPF 15 or higher and other protection measures including Limit time in sun, especially from 10am-2pm • Wear long-sleeved shirts, pants, hats and sunglasses
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Inactive Ingredients
Acetyl Hexapeptide 8, Acrylates Copolymer, a-Lipoic Acid, Aloe Barbadensis (Aloe Vera) Leaf Juice, Ascorbyl Palmitate (Vitamin C), Camellia Sinesis (Green Tea) Leaf Extract, Caprylic/Capric Triglycerides, Carthamus Tinctorius (Safflower) Oleosomes, Cetearyl Olivate, Cetyl Alcohol, Cucumis Satives (Cucumber) Fruit Extract, Dimethicone, Ethylhexylglycerin, Glycerin, Glyceryl Stearate SE, Glycyrrhiza Glabra (Licorice) Extract, Helianthus Annuus (Sunflower) Seed Oil, Linoleic Acid, Phenoxyethanol, Polysorbate 20, Sodium Hyaluronate (Hyaluronic Acid), Sodium Hydroxide, Sorbitan Olivate, Stearyl Alcohol, Tocopheryl Acetate (Vitamin E), Water
- Other Information
- Product Label
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INGREDIENTS AND APPEARANCE
KISS MY FACE SUNSCREEN FACE FACTOR BROAD SPECTRUM SPF 30
octinoxate, octisalate, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65364-210 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 30 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309) CETEARYL OLIVATE (UNII: 58B69Q84JO) CETYL ALCOHOL (UNII: 936JST6JCN) CUCUMBER (UNII: YY7C30VXJT) DIMETHICONE (UNII: 92RU3N3Y1O) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) SUNFLOWER OIL (UNII: 3W1JG795YI) LINOLEIC ACID (UNII: 9KJL21T0QJ) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBITAN OLIVATE (UNII: MDL271E3GR) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65364-210-59 1 in 1 CARTON 02/08/2017 1 59 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/09/2015 Labeler - Kiss My Face LLC (041794279)