Label: MULTIVITAMIN BODYBLOCK SPF 20- avobenzone, octinoxate, octisalate, and oxybenzone lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 21839-101-25 - Packager: Gordon Laboratories, Inc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 19, 2012
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- 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.
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- 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)
