NU SKIN TRI-PHASIC WHITE DAY MILK BROAD SPECTRUM SPF 15- avobenzone, octinoxate, and octisalate lotion 
NSE Products, Inc.

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.

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NU SKIN
Tri-Phasic White®

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?

1-888-742-7626

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
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)

Revised: 12/2022
Document Id: 0f66735b-c897-4fde-917a-e8adfba4121f
Set id: 9e104ad0-088a-47ee-a037-3c9fa3af797c
Version: 4
Effective Time: 20221216
 
NSE Products, Inc.