Nu Skin Nu Colour description, usages, side effects, indications, overdosage, supplying and lots more!

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Nu Skin Nu Colour

NSE Products, Inc.

Nu Skin Nu Colour Tinted Moisturizer Broad Spectrum SPF 15


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredients

Octinoxate (5%), Octisalate (2%).

Purpose

Sunscreen

Nu Skin Nu Colour 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.)

Nu Skin Nu Colour

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.)

Nu Skin Nu Colour

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.)

Nu Skin Nu Colour

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.)

Nu Skin Nu Colour

Nu Skin Nu Colour

Octinoxate and Octisalate LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62839-1104
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 50 mg
OCTISALATE OCTISALATE 20 mg

Inactive Ingredients

Ingredient Name Strength
HAMAMELIS VIRGINIANA TOP WATER
CYCLOMETHICONE 5
titanium dioxide
cyclomethicone
CYCLOMETHICONE 6
BUTYLENE GLYCOL
PHENYL TRIMETHICONE
NYLON-12
HEXYL LAURATE
POLYGLYCERYL-4 ISOSTEARATE
SODIUM CHLORIDE
FERRIC OXIDE YELLOW
PHENOXYETHANOL
DISTEARDIMONIUM HECTORITE
ferric oxide red
FERROSOFERRIC OXIDE
METHYLPARABEN
PROPYLENE CARBONATE
DIMETHICONE
EDETATE DISODIUM
PROPYLPARABEN
Aloe Vera Leaf
TETRAHEXYLDECYL ASCORBATE
.ALPHA.-TOCOPHEROL ACETATE
VITAMIN A PALMITATE
CORN OIL
CHROMIC OXIDE

Packaging

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

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-01-03


Nu Skin Nu Colour

Octinoxate and Octisalate LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62839-1101
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 50 mg
OCTISALATE OCTISALATE 20 mg

Inactive Ingredients

Ingredient Name Strength
HAMAMELIS VIRGINIANA TOP WATER
CYCLOMETHICONE 5
titanium dioxide
cyclomethicone
CYCLOMETHICONE 6
BUTYLENE GLYCOL
PHENYL TRIMETHICONE
NYLON-12
HEXYL LAURATE
POLYGLYCERYL-4 ISOSTEARATE
SODIUM CHLORIDE
PHENOXYETHANOL
DISTEARDIMONIUM HECTORITE
FERRIC OXIDE YELLOW
METHYLPARABEN
ferric oxide red
PROPYLENE CARBONATE
DIMETHICONE
EDETATE DISODIUM
PROPYLPARABEN
FERROSOFERRIC OXIDE
Aloe Vera Leaf
TETRAHEXYLDECYL ASCORBATE
.ALPHA.-TOCOPHEROL ACETATE
VITAMIN A PALMITATE
CORN OIL
CHROMIC OXIDE

Packaging

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

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-01-03


Nu Skin Nu Colour

Octinoxate and Octisalate LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62839-1103
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 50 mg
OCTISALATE OCTISALATE 20 mg

Inactive Ingredients

Ingredient Name Strength
HAMAMELIS VIRGINIANA TOP WATER
CYCLOMETHICONE 5
titanium dioxide
cyclomethicone
CYCLOMETHICONE 6
BUTYLENE GLYCOL
PHENYL TRIMETHICONE
NYLON-12
HEXYL LAURATE
POLYGLYCERYL-4 ISOSTEARATE
SODIUM CHLORIDE
FERRIC OXIDE YELLOW
PHENOXYETHANOL
DISTEARDIMONIUM HECTORITE
ferric oxide red
METHYLPARABEN
FERROSOFERRIC OXIDE
PROPYLENE CARBONATE
DIMETHICONE
EDETATE DISODIUM
PROPYLPARABEN
Aloe Vera Leaf
TETRAHEXYLDECYL ASCORBATE
.ALPHA.-TOCOPHEROL ACETATE
VITAMIN A PALMITATE
CORN OIL
CHROMIC OXIDE

Packaging

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

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-01-03


Nu Skin Nu Colour

Octinoxate and Octisalate LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62839-1102
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 50 mg
OCTISALATE OCTISALATE 20 mg

Inactive Ingredients

Ingredient Name Strength
HAMAMELIS VIRGINIANA TOP WATER
CYCLOMETHICONE 5
titanium dioxide
cyclomethicone
CYCLOMETHICONE 6
BUTYLENE GLYCOL
PHENYL TRIMETHICONE
NYLON-12
HEXYL LAURATE
POLYGLYCERYL-4 ISOSTEARATE
SODIUM CHLORIDE
FERRIC OXIDE YELLOW
PHENOXYETHANOL
DISTEARDIMONIUM HECTORITE
ferric oxide red
METHYLPARABEN
FERROSOFERRIC OXIDE
PROPYLENE CARBONATE
DIMETHICONE
EDETATE DISODIUM
PROPYLPARABEN
Aloe Vera Leaf
TETRAHEXYLDECYL ASCORBATE
.ALPHA.-TOCOPHEROL ACETATE
VITAMIN A PALMITATE
CORN OIL
CHROMIC OXIDE

Packaging

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

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-01-03


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Be sure to consult your doctor before taking any medication!
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