MOISTURE RESTORE DAY PROTECTIVE MATTEFYING BROAD SPECTRUM SPF15 COMBINATION TO OILY- octinoxate, octisalate, and titanium dioxide lotion

Moisture Restore Day Protective Mattefying Broad Spectrum SPF15 Combination to Oily by

Drug Labeling and Warnings

Moisture Restore Day Protective Mattefying Broad Spectrum SPF15 Combination to Oily by is a Otc medication manufactured, distributed, or labeled by NSE Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

Octinoxate (7.5%), Octisalate (3.0%), Titanium Dioxide (2.8%)

Purpose

Sunscreen

Uses

• Helps prevent sunburn. Higher SPF gives more sunburn protection
• 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.

Warning

• For external use only.

• Do not use on damaged or broken skin

• Stop use and ask a doctor if rash occurs

• When using this product, keep out of eyes. Rinse with water to remove.

• Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Using fingertips, apply generously to clean face and neck in an upward, outward motion. Use every morning before makeup application.
• Sunprotection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF of 15 or higher and other sun protection measures including:
  • Limit time in the sun, especially from 10 a.m. -2p.m.
  • Wear long-sleeved shirts, pants, hats, and sunglasses.
  • Apply liberally 15 minutes before sun exposure
  • Use a water resistant sunscreen if swimming or sweating
  • Reapply at least every 2 hours
  • Children under 6 months: Ask a doctor.

Inactive Ingredients

Water (Aqua), Butylene Glycol, Polymethyl Methacrylate, Polysorbate 40, Microcrystalline Cellulose, Corn Starch Modified, Sorbitan Oleate, Glycerin, Potassium Cetyl Phosphate, Dunaliella Salina Extract, Sodium Hyaluronate, Biosaccharide Gum-1, Glyceryl Stearate, PEG-100 Stearate, Silica, Cyclopentasiloxane, Cetyl Alcohol, Dimethicone, Hydrogenated Polydecene, Cyclohexasiloxane, PEG/PPG-18/18 Dimethicone, Xanthan Gum, Cellulose Gum, Disodium EDTA, Phytic Acid, Aminomethyl Propanol, Fragrance (Parfum), Phenoxyethanol, Chlorphenesin, Benzoic Acid.

Other Information

• Protect this product from excessive heat and direct sun.

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Carton

NU SKIN®

moisture restore
day

protective
mattefying lotion
broad spectrum
SPF 15

combination to
oily skin

50 ml e (1.7 fl. oz.)

INGREDIENTS AND APPEARANCE

MOISTURE RESTORE DAY PROTECTIVE MATTEFYING BROAD SPECTRUM SPF15 COMBINATION TO OILY 
octinoxate, octisalate, and titanium dioxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0272
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	30 mg  in 1 mL
Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP)	Titanium Dioxide	28 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Polysorbate 40 (UNII: STI11B5A2X)
Microcrystalline Cellulose (UNII: OP1R32D61U)
Glycerin (UNII: PDC6A3C0OX)
Sorbitan Monooleate (UNII: 06XEA2VD56)
Potassium Cetyl Phosphate (UNII: 03KCY6P7UT)
Dunaliella Salina (UNII: F4O1DKI9A6)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Biosaccharide Gum-1 (UNII: BB4PU4V09H)
Glyceryl Monostearate (UNII: 230OU9XXE4)
PEG-100 Stearate (UNII: YD01N1999R)
Silicon Dioxide (UNII: ETJ7Z6XBU4)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Cetyl Alcohol (UNII: 936JST6JCN)
Dimethicone (UNII: 92RU3N3Y1O)
HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
Cyclomethicone 6 (UNII: XHK3U310BA)
Xanthan Gum (UNII: TTV12P4NEE)
Carboxymethylcellulose Sodium, Unspecified Form (UNII: K679OBS311)
Edetate Disodium (UNII: 7FLD91C86K)
Fytic Acid (UNII: 7IGF0S7R8I)
Aminomethylpropanol (UNII: LU49E6626Q)
Phenoxyethanol (UNII: HIE492ZZ3T)
Chlorphenesin (UNII: I670DAL4SZ)
Benzoic Acid (UNII: 8SKN0B0MIM)
Methylparaben (UNII: A2I8C7HI9T)
Propylparaben (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0272-7	1 in 1 CARTON	06/10/2001
1		50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	06/10/2001

Labeler - NSE Products, Inc. (803486393)