Label: SUNPLUS SPF50 FACE BODY SUNSCREEN- sunscreen lotion
- NDC Code(s): 65112-304-01
- Packager: I.Shay Cosmetics
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 13, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
INACTIVE INGREDIENT
Purified Water, Glycerin, Ceteareth-20, Cetearyl Alcohol, Dimethicone, Glyceryl stearate, PEG-100, Acrylic Polymer, Cetyl Alcohol, Potassium Hexadecyl Phosphate, PEG 300, Grapeseed Oil, Sunflower Oil, Safflower Oil, Organic Borage Oil, Organic Evening Primrose Oil, Allantoin, Hyaluronic Acid, Organic Raspberry Seed Oil, Organic Jojoba Oil, Organic Aloe Oil, Phenoxyethanol, Ethylhexylglycerin
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SUNPLUS SPF50 FACE BODY SUNSCREEN
sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65112-304 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 0.06 g in 118 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 0.05 g in 118 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 0.15 g in 118 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 0.02 g in 118 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65112-304-01 118 mL in 1 TUBE; Type 0: Not a Combination Product 06/01/2004 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/01/2004 Labeler - I.Shay Cosmetics (151582384)