Label: NO BS MOISTURIZER SPF20- octinoxate, octisalate, avobenzone lotion
- NDC Code(s): 71852-334-00
- Packager: Product Management, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 5, 2023
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- DRUG FACTS
- Active Ingredients
- USES:
- WARNINGS:
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DIRECTIONS:
• Apply liberally 15 minutes before sun exposure. • Reapply: - At least every two hours. - Immediately after swimming, sweating, or towel drying.
Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun protection measures including: - Limit time in the sun, especially between 10am and 2pm. - Wear long sleeve shirts, pants, hats, and sunglasses. - For children under six months, consult a physician. SUN PROTECTION MEASURES:
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OTHER INGREDIENTS:
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Algae Extract, C12-15 Alkyl Benzoate, Aqua (Deionized Water), Butylene Glycol, Butyrospermum Parkii (Shea) Butter, Camellia Sinensis (Green Tea) Leaf Extract, Caprylic/Capric Triglyceride, Carbomer, Cetearyl Alcohol, Cetearyl Glucoside, Citrus Aurantium Dulcis (Orange) Oil, Cocos Nucifera (Coconut) Oil, Ethoxydiglycol, Ethylhexylglycerin, Fucus Vesiculosus (Seaweed) Extract, Glycerin, Hyaluronic Acid, Hydrolyzed Collagen, Isopropyl Myristate, Isostearyl Palmitate, Mangifera Indica (Mango) Seed Butter, Moringa Oleifera (Moringa) Oil, Palmitoyl Oligopeptide, Palmitoyl Tetrapeptide-7, Phenoxyethanol, Polysorbate 20, Punica Granatum (Pomegranate) Extract, Retinol (Vitamin A), Saccharide Isomerate, Sodium Hydroxide, Sodium PCA, Tetrahexyldecyl Ascorbate (Vitamin C), Theobroma Cacao (Cocoa) Seed Butter, Tocopheryl Acetate (Vitamin E).
- OTHER INFORMATION:
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NO BS MOISTURIZER SPF20
octinoxate, octisalate, avobenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71852-334 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 50 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 30 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SHEA BUTTER (UNII: K49155WL9Y) GREEN TEA LEAF (UNII: W2ZU1RY8B0) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) ORANGE OIL (UNII: AKN3KSD11B) COCONUT OIL (UNII: Q9L0O73W7L) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) NORI (UNII: 477TV3P5UX) GLYCERIN (UNII: PDC6A3C0OX) HYALURONIC ACID (UNII: S270N0TRQY) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ISOSTEARYL PALMITATE (UNII: 9EHU0R7ER1) MANGIFERA INDICA SEED BUTTER (UNII: 4OXD9M35X2) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) POMEGRANATE (UNII: 56687D1Z4D) RETINOL (UNII: G2SH0XKK91) SACCHARIDE ISOMERATE (UNII: W8K377W98I) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) COCOA BUTTER (UNII: 512OYT1CRR) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71852-334-00 1 in 1 BOX 06/01/2018 1 50 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/01/2018 Labeler - Product Management, LLC (080906171) Establishment Name Address ID/FEI Business Operations Pure Source, LLC 080354456 manufacture(71852-334)