Label: NU SKIN TRI-PHASIC WHITE DAY MILK BROAD SPECTRUM SPF 15- avobenzone, octinoxate, and octisalate lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 December 16, 2022

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  • Active Ingredients

    Avobenzone (2.4%), Octinoxate (7.4%), Octisalate (3.0%).

  • Warnings

    For external use only.

    Discontinue use if irritation occurs.

  • Directions

    Use in the morning after applying Tri-Phasic White Essence. Apply liberally to face and neck.

  • Inactive Ingredients

    Water (Aqua), Cyclomethicone, Butylene Glycol, Bis-PEG/PPG-16/16 PEG/PPG-16/16 Dimethicone, Octyldodecyl Neopentanoate, Glycerin, Squalane, Hexapeptide-2, Caprylic/Capric Triglyceride, Phenyl Trimethicone, Tocopheryl Acetate, Allantoin, Phospholipids, Xanthan Gum, Dimethiconol, Dextran, Polyphosphorylcholine Glycol Acrylate, Polysorbate 80, PEG-8, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polysorbate 60, Aminomethyl Propanol, Disodium EDTA, Fragrance (Parfum), Phenoxyethanol, Chlorphenesin, Methylparaben, Benzoic Acid.

  • Questions?

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  • PRINCIPAL DISPLAY PANEL - 75 ml Bottle Carton

    NU SKIN

    Tri-Phasic White®

    DAY MILK LOTION
    BROAD SPECTRUM
    SPF 15

    75 ml e (2.5 fl. oz.)

    Principal Display Panel - 75 ml Bottle Carton
  • INGREDIENTS AND APPEARANCE
    NU SKIN TRI-PHASIC WHITE DAY MILK BROAD SPECTRUM SPF 15 
    avobenzone, octinoxate, and octisalate lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62839-0273
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone24 mg  in 1 mL
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate74 mg  in 1 mL
    Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Cyclomethicone (UNII: NMQ347994Z)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Octyldodecyl Neopentanoate (UNII: X8725R883T)  
    Glycerin (UNII: PDC6A3C0OX)  
    Squalane (UNII: GW89575KF9)  
    Medium-Chain Triglycerides (UNII: C9H2L21V7U)  
    Phenyl Trimethicone (UNII: DR0K5NOJ4R)  
    Allantoin (UNII: 344S277G0Z)  
    Xanthan Gum (UNII: TTV12P4NEE)  
    Polysorbate 80 (UNII: 6OZP39ZG8H)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    Polysorbate 60 (UNII: CAL22UVI4M)  
    Aminomethylpropanol (UNII: LU49E6626Q)  
    Edetate Disodium (UNII: 7FLD91C86K)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Chlorphenesin (UNII: I670DAL4SZ)  
    Methylparaben (UNII: A2I8C7HI9T)  
    Benzoic Acid (UNII: 8SKN0B0MIM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62839-0273-11 in 1 CARTON04/01/2013
    175 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Not Finalpart35204/01/2013
    Labeler - NSE Products, Inc. (803486393)
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