NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 BEIGE- octinoxate and octisalate lotion NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 FAIR- octinoxate and octisalate lotion NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 HONEY- octinoxate and octisalate lotion NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 SAND- octinoxate and octisalate lotion

Nu Skin Nu Colour by

Drug Labeling and Warnings

Nu Skin Nu Colour 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 (5%), Octisalate (2%).

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

• Shake well before use. Smooth over face and neck area blending well. Seal with powder if desired.
• 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.

Other Information

• Protect this product from excessive heat and direct sun.

Inactive Ingredients

Hamamelis Virginiana (Witch Hazel) Water, Cyclopentasiloxane, Titanium Dioxide (Cl 77891), Cyclomethicone, Dimethicone Crosspolymer, Cyclohexasiloxane, Butylene Glycol, Phenyl Trimethicone, Nylon-12, Hexyl Laurate, Cetyl PEG/PPG-10/1 Dimethicone, Polyglyceryl-4 Isostearate, Sodium Chloride, Aloe Barbadensis Leaf Juice, Retinyl Palmitate, Tocopheryl Acetate, Tetrahexyldecyl Ascorbate, Zea Mays (Corn) Oil, Methicone, Dimethicone, Disteardimonium Hectorite, Propylene Carbonate, Disodium EDTA, Fragrance, Phenoxyethanol, Methylparaben, Propylparaben.

May Contain

Iron Oxides (CI 77491, CI 77492, CI 77499), Chromium Oxide Greens (CI 77288).

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton (Beige)

Nu Colour®

Tinted Moisturizer

Broad Spectrum
SPF 15

NU SKIN®

40 ml e (1.4 fl.oz.)

PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton (Fair)

Nu Colour®

Tinted Moisturizer

Broad Spectrum
SPF 15

NU SKIN®

40 ml e (1.4 fl.oz.)

PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton (Honey)

Nu Colour®

Tinted Moisturizer

Broad Spectrum
SPF 15

NU SKIN®

40 ml e (1.4 fl.oz.)

PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton (Sand)

Nu Colour®

Tinted Moisturizer

Broad Spectrum
SPF 15

NU SKIN®

40 ml e (1.4 fl.oz.)

INGREDIENTS AND APPEARANCE

NU SKIN NU COLOUR   TINTED MOISTURIZER BROAD SPECTRUM SPF 15 BEIGE
octinoxate and octisalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-1104
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	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Hamamelis Virginiana Top Water (UNII: NT00Y05A2V)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Titanium Dioxide (UNII: 15FIX9V2JP)
Cyclomethicone (UNII: NMQ347994Z)
Cyclomethicone 6 (UNII: XHK3U310BA)
Butylene Glycol (UNII: 3XUS85K0RA)
Phenyl Trimethicone (UNII: DR0K5NOJ4R)
Nylon-12 (UNII: 446U8J075B)
Hexyl Laurate (UNII: 4CG9F9W01Q)
Polyglyceryl-4 Isostearate (UNII: 820DPX33S7)
Sodium Chloride (UNII: 451W47IQ8X)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Phenoxyethanol (UNII: HIE492ZZ3T)
Disteardimonium Hectorite (UNII: X687XDK09L)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)
Methylparaben (UNII: A2I8C7HI9T)
Propylene Carbonate (UNII: 8D08K3S51E)
Dimethicone (UNII: 92RU3N3Y1O)
Edetate Disodium (UNII: 7FLD91C86K)
Propylparaben (UNII: Z8IX2SC1OH)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Vitamin A Palmitate (UNII: 1D1K0N0VVC)
Corn Oil (UNII: 8470G57WFM)
Chromic Oxide (UNII: X5Z09SU859)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-1104-1	1 in 1 CARTON
1		40 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	01/03/2011

NU SKIN NU COLOUR   TINTED MOISTURIZER BROAD SPECTRUM SPF 15 FAIR
octinoxate and octisalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-1101
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	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Hamamelis Virginiana Top Water (UNII: NT00Y05A2V)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Titanium Dioxide (UNII: 15FIX9V2JP)
Cyclomethicone (UNII: NMQ347994Z)
Cyclomethicone 6 (UNII: XHK3U310BA)
Butylene Glycol (UNII: 3XUS85K0RA)
Phenyl Trimethicone (UNII: DR0K5NOJ4R)
Nylon-12 (UNII: 446U8J075B)
Hexyl Laurate (UNII: 4CG9F9W01Q)
Polyglyceryl-4 Isostearate (UNII: 820DPX33S7)
Sodium Chloride (UNII: 451W47IQ8X)
Phenoxyethanol (UNII: HIE492ZZ3T)
Disteardimonium Hectorite (UNII: X687XDK09L)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Methylparaben (UNII: A2I8C7HI9T)
Ferric Oxide Red (UNII: 1K09F3G675)
Propylene Carbonate (UNII: 8D08K3S51E)
Dimethicone (UNII: 92RU3N3Y1O)
Edetate Disodium (UNII: 7FLD91C86K)
Propylparaben (UNII: Z8IX2SC1OH)
Ferrosoferric Oxide (UNII: XM0M87F357)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Vitamin A Palmitate (UNII: 1D1K0N0VVC)
Corn Oil (UNII: 8470G57WFM)
Chromic Oxide (UNII: X5Z09SU859)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-1101-1	1 in 1 CARTON
1		40 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	01/03/2011

NU SKIN NU COLOUR   TINTED MOISTURIZER BROAD SPECTRUM SPF 15 HONEY
octinoxate and octisalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-1103
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	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Hamamelis Virginiana Top Water (UNII: NT00Y05A2V)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Titanium Dioxide (UNII: 15FIX9V2JP)
Cyclomethicone (UNII: NMQ347994Z)
Cyclomethicone 6 (UNII: XHK3U310BA)
Butylene Glycol (UNII: 3XUS85K0RA)
Phenyl Trimethicone (UNII: DR0K5NOJ4R)
Nylon-12 (UNII: 446U8J075B)
Hexyl Laurate (UNII: 4CG9F9W01Q)
Polyglyceryl-4 Isostearate (UNII: 820DPX33S7)
Sodium Chloride (UNII: 451W47IQ8X)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Phenoxyethanol (UNII: HIE492ZZ3T)
Disteardimonium Hectorite (UNII: X687XDK09L)
Ferric Oxide Red (UNII: 1K09F3G675)
Methylparaben (UNII: A2I8C7HI9T)
Ferrosoferric Oxide (UNII: XM0M87F357)
Propylene Carbonate (UNII: 8D08K3S51E)
Dimethicone (UNII: 92RU3N3Y1O)
Edetate Disodium (UNII: 7FLD91C86K)
Propylparaben (UNII: Z8IX2SC1OH)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Vitamin A Palmitate (UNII: 1D1K0N0VVC)
Corn Oil (UNII: 8470G57WFM)
Chromic Oxide (UNII: X5Z09SU859)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-1103-1	1 in 1 CARTON
1		40 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	01/03/2011

NU SKIN NU COLOUR   TINTED MOISTURIZER BROAD SPECTRUM SPF 15 SAND
octinoxate and octisalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-1102
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	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Hamamelis Virginiana Top Water (UNII: NT00Y05A2V)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Titanium Dioxide (UNII: 15FIX9V2JP)
Cyclomethicone (UNII: NMQ347994Z)
Cyclomethicone 6 (UNII: XHK3U310BA)
Butylene Glycol (UNII: 3XUS85K0RA)
Phenyl Trimethicone (UNII: DR0K5NOJ4R)
Nylon-12 (UNII: 446U8J075B)
Hexyl Laurate (UNII: 4CG9F9W01Q)
Polyglyceryl-4 Isostearate (UNII: 820DPX33S7)
Sodium Chloride (UNII: 451W47IQ8X)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Phenoxyethanol (UNII: HIE492ZZ3T)
Disteardimonium Hectorite (UNII: X687XDK09L)
Ferric Oxide Red (UNII: 1K09F3G675)
Methylparaben (UNII: A2I8C7HI9T)
Ferrosoferric Oxide (UNII: XM0M87F357)
Propylene Carbonate (UNII: 8D08K3S51E)
Dimethicone (UNII: 92RU3N3Y1O)
Edetate Disodium (UNII: 7FLD91C86K)
Propylparaben (UNII: Z8IX2SC1OH)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Vitamin A Palmitate (UNII: 1D1K0N0VVC)
Corn Oil (UNII: 8470G57WFM)
Chromic Oxide (UNII: X5Z09SU859)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-1102-1	1 in 1 CARTON
1		40 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	01/03/2011

Labeler - NSE Products, Inc. (803486393)