NDC | 11410-150-11, 11410-160-22 |
Set ID | 4eb53e43-8a20-4b10-9612-ed4ec08b56ac |
Category | HUMAN OTC DRUG LABEL |
Packager | Guthy-Renker LLC |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- SPL UNCLASSIFIED SECTION
- Directions
- WARNINGS
- Active Ingredients
-
Other Ingredients
Water (Aqua), Glycolic Acid, Glycerin, Ammonium Hydroxide, Steareth-20, Hexyl Laurate, Dimethicone, Steareth-2, Cetyl Alcohol, DEA-Cetyl Phosphate, PEG-100 Stearate, Methyl Methacrylate Crosspolymer, Camellia Oleifera Leaf Extract, Ormenis Multicaulis Oil, Tocopheryl Acetate, Allantoin, Panthenol, Butylene Glycol, Propylene Glycol, Glyceryl Stearate, Octyldodecyl Neopentanoate, Stearic Acid, Magnesium Aluminum Silicate, Xanthan Gum, Disodium EDTA, Diazolidinyl Urea, Methylparaben, Propylparaben, Aluminum Hydroxide, (CI 77002), Titanium Dioxide (CI 77891)
- PRINCIPAL DISPLAY PANEL - 30 ml Tube
- PRINCIPAL DISPLAY PANEL - 50 ml Tube
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INGREDIENTS AND APPEARANCE
JANE SEYMOUR NATURAL ADVANTAGE AM SPF 15 ALL DAY MOISTURE WITH AHAS
octinoxate, oxybenzone, and octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11410-150 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.075 mL in 1 mL Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone 0.04 mg in 1 mL Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 0.035 mL in 1 mL Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11410-150-11 30 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part352 04/26/2005 JANE SEYMOUR NATURAL ADVANTAGE AM SPF 15 ALL DAY MOISTURE WITH AHAS
octinoxate, oxybenzone, and octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11410-160 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.075 mL in 1 mL Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone 0.04 mg in 1 mL Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 0.035 mL in 1 mL Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11410-160-22 50 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part352 04/26/2005 Labeler - Guthy-Renker LLC (608315453)