NDC | 75936-506-01, 75936-506-02, 75936-506-03, 75936-506-04 |
Set ID | 7c265e0e-62cb-ba21-e053-2a91aa0a2be3 |
Category | HUMAN OTC DRUG LABEL |
Packager | TAYLOR JAMES, LTD. |
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 generously and evenly 15 minutes before sun exposure
- reapply at least every 2 hours
- Use a water resistant sunscreen if swimming or sweating
- Sun Protection Measure 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 value of 15 or higher and other sun protection measures including:
- Limit time in the sun, especially from 10 a.m. - 2p.m.
- Wear Long-sleeved shirts, pants hats and sunglasses
- Children under 6 months ask a doctor
-
INACTIVE INGREDIENT
Inactive ingredients Water, Cartamus Tinctorius (safflower) Olesomes, Glycerin, C12-15 Alkyl Benzoate, Polyester-7, Ammonium Acryloyldimethyldimethyltaurate/VP Copolymer, Neopentyl Glycol Diheptanoate, Carthamus Tinctorius (Safflower) Seedcake extract, Aphanizomenon Flos-Aquae Extract, Inulin Lauryl Carbamate, Xanthan Gum, Biosaccharide Gum-4, Cerium Oxide, Platinum Powder, 1,2-hexanediol, Ehtylhexylglycerin, Phenethyl Alcohol, Chlorphenesin
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SUPERSCREEN DAILY MOISTURIZER BROAD SPECTRUM SPF 40
avobenzone,homosalate, octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75936-506 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 8 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 8 g in 100 mL Inactive Ingredients Ingredient Name Strength POLYESTER-7 (UNII: 0841698D2F) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) CARTHAMUS TINCTORIUS SEEDCAKE (UNII: DHQ13F4N2W) CERIC OXIDE (UNII: 619G5K328Y) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) PLATINUM (UNII: 49DFR088MY) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CHLORPHENESIN (UNII: I670DAL4SZ) APHANIZOMENON FLOSAQUAE (UNII: 49VG1X560X) BIOSACCHARIDE GUM-4 (UNII: 9XRL057X90) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309) GLYCERIN (UNII: PDC6A3C0OX) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75936-506-01 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/01/2018 2 NDC:75936-506-02 15 mL in 1 JAR; Type 0: Not a Combination Product 12/01/2018 3 NDC:75936-506-03 10 mL in 1 JAR; Type 0: Not a Combination Product 12/01/2018 4 NDC:75936-506-04 1.5 mL in 1 PACKET; Type 0: Not a Combination Product 12/01/2018 09/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 12/01/2018 Labeler - TAYLOR JAMES, LTD. (033381850)