NDC | 21839-101-25 |
Set ID | c9100083-55b0-4301-b031-e5f11f5b86e3 |
Category | HUMAN OTC DRUG LABEL |
Packager | Gordon Laboratories, Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- active ingredients
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other ingredients
Water, Caprylic/Capric Triglyceride, Isopropyl Isostearate, Butylene Glycol, Cetearyl Alcohol, Cetyl Dimethicone, Phenoxyethanol, Butyrospermum Parkii (Shea Butter), Polysorbate 60, Ceteareth-20, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Lavandula Hybrida Oil, Dicetyl Phosphate, Ceteth-10 Phosphate, Methylparaben, Linalool, Propylparaben, Chlorphenesin, Lavandula Angustifolia (Lavender) Extract, Oenothera Biennis (Evening Primrose) Oil, Panthenol, Tocopheryl Acetate, Glycolipids, Sodium Hyaluronate, Carbomer, Disodium EDTA, Ascorbyl Tetraisopalmitate, Sodium DNA, Tocopherol, Ascorbyl Palmitate, Limonene.
- warnings
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 125 ml Tube Box
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INGREDIENTS AND APPEARANCE
MULTIVITAMIN BODYBLOCK SPF 20
avobenzone, octinoxate, octisalate, and oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21839-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone 2.5 mL in 125 mL Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 9.4 mL in 125 mL Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 6.25 mL in 125 mL Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone 3.75 mL in 125 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Medium-Chain Triglycerides (UNII: C9H2L21V7U) Isopropyl Isostearate (UNII: C67IXB9Y7T) Butylene Glycol (UNII: 3XUS85K0RA) Cetostearyl Alcohol (UNII: 2DMT128M1S) Phenoxyethanol (UNII: HIE492ZZ3T) Shea Butter (UNII: K49155WL9Y) Polysorbate 60 (UNII: CAL22UVI4M) Polyoxyl 20 Cetostearyl Ether (UNII: YRC528SWUY) Aminomethylpropanol (UNII: LU49E6626Q) Lavandin Oil (UNII: 9RES347CKG) Dihexadecyl Phosphate (UNII: 2V6E5WN99N) Ceteth-10 Phosphate (UNII: 4E05O5N49G) Methylparaben (UNII: A2I8C7HI9T) Linalool, (+/-)- (UNII: D81QY6I88E) Propylparaben (UNII: Z8IX2SC1OH) Chlorphenesin (UNII: I670DAL4SZ) Lavandula Angustifolia Flowering Top (UNII: 9YT4B71U8P) Evening Primrose Oil (UNII: 3Q9L08K71N) Panthenol (UNII: WV9CM0O67Z) Alpha-Tocopherol Acetate (UNII: 9E8X80D2L0) Hyaluronate Sodium (UNII: YSE9PPT4TH) Edetate Disodium (UNII: 7FLD91C86K) Tocopherol (UNII: R0ZB2556P8) Ascorbyl Palmitate (UNII: QN83US2B0N) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21839-101-25 1 in 1 BOX 1 125 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part352 11/01/2005 Labeler - Gordon Laboratories, Inc (008328619)