Label: 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
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Contains inactivated NDC Code(s)
NDC Code(s): 62839-1101-1, 62839-1102-1, 62839-1103-1, 62839-1104-1 - Packager: NSE Products, Inc.
- 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 June 19, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
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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
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Directions
- Shake well before use. Smooth over face and neck area blending well. Seal with powder if desired.
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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
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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.
- Questions?
- PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton (Beige)
- PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton (Fair)
- PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton (Honey)
- PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton (Sand)
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INGREDIENTS AND APPEARANCE
NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 BEIGE
octinoxate and octisalate lotionProduct 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 lotionProduct 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 lotionProduct 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 lotionProduct 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)
