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

If you are a consumer or patient please visit this version.

  • DRUG FACTS

  • Active Ingredients

    Octinoxate 5.00%

    Octisalate 3.00%

    Avobenzone 3.00%

    Purpose

    Sunscreen

  • USES:

    • Helps prevent sunburn. • If used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging caused by the sun.

  • WARNINGS:

    • For external use only.

    Do not use

    • on damaged or broken skin.

    When using this product

    • keep out of eyes.  Rinse with water to remove.

    Stop use and consult physician

    • if irritation  or rash develops.

    Keep out of reach of children. 

    If product is swallowed, get medical attention or contact poison control center immediately.

  • 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:


  • 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:

    • Protect this product from excessive heat and direct sunlight.

  • PRINCIPAL DISPLAY PANEL

    Outer PackageInner Package

  • INGREDIENTS AND APPEARANCE
    NO BS MOISTURIZER SPF20 
    octinoxate, octisalate, avobenzone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71852-334
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE50 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE30 mg  in 1 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71852-334-001 in 1 BOX06/01/2018
    150 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/01/2018
    Labeler - Product Management, LLC (080906171)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pure Source, LLC080354456manufacture(71852-334)