Label: NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - BEIGE- octinoxate and octisalate lotion
NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - FAIR- octinoxate and octisalate lotion
NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - HONEY- octinoxate and octisalate lotion
NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - MEDIUM BEIGE- octinoxate and octisalate lotion
NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - MEDIUM OCHRE- octinoxate and octisalate lotion
NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - NATURAL BEIGE- octinoxate and octisalate lotion
NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - OCHRE- octinoxate and octisalate lotion
NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - PINK- octinoxate and octisalate lotion
NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - PINK OCHRE- octinoxate and octisalate lotion
NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - SAND- octinoxate and octisalate lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 62839-1113-1, 62839-1114-1, 62839-1115-1, 62839-1116-1, view more62839-1135-1, 62839-1136-1, 62839-1137-1, 62839-1138-1, 62839-1139-1, 62839-1140-1 - Packager: NSE Products, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 3, 2025
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
-
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
-
Directions
- Shake well before use. Smooth over face and neck area, blending well. Seal with powder if desired.
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Sun Protection 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.–2 p.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 two hours.
- Children under 6 months: Ask a doctor.
- Other Information
-
Inactive Ingredients
Hamamelis Virginiana (Witch Hazel) Water, Cyclopentasiloxane, Butylene Glycol, Cyclomethicone, Dimethicone Crosspolymer, Cyclohexasiloxane, Phenyl Trimethicone, Nylon-12, Hexyl Laurate, Cetyl PEG/PPG-10/1 Dimethicone, Polyglyceryl-4 Isostearate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Tetrahexyldecyl Ascorbate, Nylon-12 Fluorescent Brightener 230 Salt, Dipalmitoyl Hydroxyproline, Propylene Carbonate, Methicone, Dimethicone, Disteardimonium Hectorite, Polyvinylalcohol Crosspolymer, Sodium Chloride, Disodium EDTA, Fragrance (Parfum), Caprylyl Glycol, Phenoxyethanol, Chlorphenesin.
May Contain:
Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, CI 77492, CI 77499), Chromium Oxide Greens.
- 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 - Medium Beige
- PRINCIPAL DISPLAY PANEL - 40 mL Bottle Carton - Medium Ochre
- PRINCIPAL DISPLAY PANEL - 40 mL Bottle Carton - Natural Beige
- PRINCIPAL DISPLAY PANEL - 40 mL Bottle Carton - Ochre
- PRINCIPAL DISPLAY PANEL - 40 mL Bottle Carton - Pink
- PRINCIPAL DISPLAY PANEL - 40 mL Bottle Carton - Pink Ochre
- PRINCIPAL DISPLAY PANEL - 40 mL Bottle Carton - Sand
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INGREDIENTS AND APPEARANCE
NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - BEIGE
octinoxate and octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-1116 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 28 mg in 1 mL Inactive Ingredients Ingredient Name Strength Hamamelis Virginiana Top Water (UNII: NT00Y05A2V) Cyclomethicone 5 (UNII: 0THT5PCI0R) Butylene Glycol (UNII: 3XUS85K0RA) Titanium Dioxide (UNII: 15FIX9V2JP) Cyclomethicone (UNII: NMQ347994Z) Cyclomethicone 6 (UNII: XHK3U310BA) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Nylon-12 (UNII: 446U8J075B) Hexyl Laurate (UNII: 4CG9F9W01Q) Polyglyceryl-4 Isostearate (UNII: 820DPX33S7) Aloe Vera Leaf (UNII: ZY81Z83H0X) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ) Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H) Propylene Carbonate (UNII: 8D08K3S51E) Dimethicone (UNII: 92RU3N3Y1O) Disteardimonium Hectorite (UNII: X687XDK09L) Sodium Chloride (UNII: 451W47IQ8X) Edetate Disodium (UNII: 7FLD91C86K) Caprylyl Glycol (UNII: 00YIU5438U) Phenoxyethanol (UNII: HIE492ZZ3T) Chlorphenesin (UNII: I670DAL4SZ) Ferric Oxide Red (UNII: 1K09F3G675) Ferric Oxide Yellow (UNII: EX438O2MRT) Ferrosoferric Oxide (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-1116-1 1 in 1 CARTON 10/27/2014 1 40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M020 10/27/2014 NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - FAIR
octinoxate and octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-1113 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 28 mg in 1 mL Inactive Ingredients Ingredient Name Strength Hamamelis Virginiana Top Water (UNII: NT00Y05A2V) Cyclomethicone 5 (UNII: 0THT5PCI0R) Butylene Glycol (UNII: 3XUS85K0RA) Titanium Dioxide (UNII: 15FIX9V2JP) Cyclomethicone (UNII: NMQ347994Z) Cyclomethicone 6 (UNII: XHK3U310BA) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Hexyl Laurate (UNII: 4CG9F9W01Q) Polyglyceryl-4 Isostearate (UNII: 820DPX33S7) Aloe Vera Leaf (UNII: ZY81Z83H0X) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ) Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H) Propylene Carbonate (UNII: 8D08K3S51E) Dimethicone (UNII: 92RU3N3Y1O) Disteardimonium Hectorite (UNII: X687XDK09L) Sodium Chloride (UNII: 451W47IQ8X) Edetate Disodium (UNII: 7FLD91C86K) Caprylyl Glycol (UNII: 00YIU5438U) Phenoxyethanol (UNII: HIE492ZZ3T) Chlorphenesin (UNII: I670DAL4SZ) Ferric Oxide Red (UNII: 1K09F3G675) Ferric Oxide Yellow (UNII: EX438O2MRT) Ferrosoferric Oxide (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-1113-1 1 in 1 CARTON 10/27/2014 1 40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M020 10/27/2014 NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - HONEY
octinoxate and octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-1115 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 28 mg in 1 mL Inactive Ingredients Ingredient Name Strength Hamamelis Virginiana Top Water (UNII: NT00Y05A2V) Cyclomethicone 5 (UNII: 0THT5PCI0R) Butylene Glycol (UNII: 3XUS85K0RA) Titanium Dioxide (UNII: 15FIX9V2JP) Cyclomethicone (UNII: NMQ347994Z) Cyclomethicone 6 (UNII: XHK3U310BA) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Hexyl Laurate (UNII: 4CG9F9W01Q) Polyglyceryl-4 Isostearate (UNII: 820DPX33S7) Aloe Vera Leaf (UNII: ZY81Z83H0X) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ) Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H) Propylene Carbonate (UNII: 8D08K3S51E) Dimethicone (UNII: 92RU3N3Y1O) Disteardimonium Hectorite (UNII: X687XDK09L) Sodium Chloride (UNII: 451W47IQ8X) Edetate Disodium (UNII: 7FLD91C86K) Caprylyl Glycol (UNII: 00YIU5438U) Phenoxyethanol (UNII: HIE492ZZ3T) Chlorphenesin (UNII: I670DAL4SZ) Ferric Oxide Red (UNII: 1K09F3G675) Ferric Oxide Yellow (UNII: EX438O2MRT) Ferrosoferric Oxide (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-1115-1 1 in 1 CARTON 10/27/2014 1 40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M020 10/27/2014 NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - MEDIUM BEIGE
octinoxate and octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-1140 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 28 mg in 1 mL Inactive Ingredients Ingredient Name Strength Hamamelis Virginiana Top Water (UNII: NT00Y05A2V) Cyclomethicone 5 (UNII: 0THT5PCI0R) Butylene Glycol (UNII: 3XUS85K0RA) Titanium Dioxide (UNII: 15FIX9V2JP) Cyclomethicone (UNII: NMQ347994Z) Cyclomethicone 6 (UNII: XHK3U310BA) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Hexyl Laurate (UNII: 4CG9F9W01Q) Polyglyceryl-4 Isostearate (UNII: 820DPX33S7) Ferric Oxide Yellow (UNII: EX438O2MRT) Aloe Vera Leaf (UNII: ZY81Z83H0X) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ) Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H) Propylene Carbonate (UNII: 8D08K3S51E) Dimethicone (UNII: 92RU3N3Y1O) Disteardimonium Hectorite (UNII: X687XDK09L) Sodium Chloride (UNII: 451W47IQ8X) Edetate Disodium (UNII: 7FLD91C86K) Caprylyl Glycol (UNII: 00YIU5438U) Phenoxyethanol (UNII: HIE492ZZ3T) Chlorphenesin (UNII: I670DAL4SZ) Ferric Oxide Red (UNII: 1K09F3G675) Ferrosoferric Oxide (UNII: XM0M87F357) Chromic Oxide (UNII: X5Z09SU859) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-1140-1 1 in 1 CARTON 10/27/2014 1 40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M020 10/27/2014 NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - MEDIUM OCHRE
octinoxate and octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-1137 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 28 mg in 1 mL Inactive Ingredients Ingredient Name Strength Hamamelis Virginiana Top Water (UNII: NT00Y05A2V) Cyclomethicone 5 (UNII: 0THT5PCI0R) Butylene Glycol (UNII: 3XUS85K0RA) Titanium Dioxide (UNII: 15FIX9V2JP) Cyclomethicone (UNII: NMQ347994Z) Cyclomethicone 6 (UNII: XHK3U310BA) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Hexyl Laurate (UNII: 4CG9F9W01Q) Polyglyceryl-4 Isostearate (UNII: 820DPX33S7) Ferric Oxide Yellow (UNII: EX438O2MRT) Aloe Vera Leaf (UNII: ZY81Z83H0X) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ) Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H) Propylene Carbonate (UNII: 8D08K3S51E) Dimethicone (UNII: 92RU3N3Y1O) Disteardimonium Hectorite (UNII: X687XDK09L) Sodium Chloride (UNII: 451W47IQ8X) Edetate Disodium (UNII: 7FLD91C86K) Caprylyl Glycol (UNII: 00YIU5438U) Phenoxyethanol (UNII: HIE492ZZ3T) Chlorphenesin (UNII: I670DAL4SZ) Ferric Oxide Red (UNII: 1K09F3G675) Ferrosoferric Oxide (UNII: XM0M87F357) Chromic Oxide (UNII: X5Z09SU859) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-1137-1 1 in 1 CARTON 10/27/2014 1 40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M020 10/27/2014 NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - NATURAL BEIGE
octinoxate and octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-1139 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 28 mg in 1 mL Inactive Ingredients Ingredient Name Strength Hamamelis Virginiana Top Water (UNII: NT00Y05A2V) Cyclomethicone 5 (UNII: 0THT5PCI0R) Butylene Glycol (UNII: 3XUS85K0RA) Titanium Dioxide (UNII: 15FIX9V2JP) Cyclomethicone (UNII: NMQ347994Z) Cyclomethicone 6 (UNII: XHK3U310BA) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Hexyl Laurate (UNII: 4CG9F9W01Q) Polyglyceryl-4 Isostearate (UNII: 820DPX33S7) Aloe Vera Leaf (UNII: ZY81Z83H0X) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ) Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H) Propylene Carbonate (UNII: 8D08K3S51E) Dimethicone (UNII: 92RU3N3Y1O) Disteardimonium Hectorite (UNII: X687XDK09L) Sodium Chloride (UNII: 451W47IQ8X) Edetate Disodium (UNII: 7FLD91C86K) Caprylyl Glycol (UNII: 00YIU5438U) Phenoxyethanol (UNII: HIE492ZZ3T) Chlorphenesin (UNII: I670DAL4SZ) Ferric Oxide Red (UNII: 1K09F3G675) Ferric Oxide Yellow (UNII: EX438O2MRT) Ferrosoferric Oxide (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-1139-1 1 in 1 CARTON 10/27/2014 1 40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M020 10/27/2014 NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - OCHRE
octinoxate and octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-1135 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 28 mg in 1 mL Inactive Ingredients Ingredient Name Strength Hamamelis Virginiana Top Water (UNII: NT00Y05A2V) Cyclomethicone 5 (UNII: 0THT5PCI0R) Butylene Glycol (UNII: 3XUS85K0RA) Titanium Dioxide (UNII: 15FIX9V2JP) Cyclomethicone (UNII: NMQ347994Z) Cyclomethicone 6 (UNII: XHK3U310BA) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Hexyl Laurate (UNII: 4CG9F9W01Q) Polyglyceryl-4 Isostearate (UNII: 820DPX33S7) Aloe Vera Leaf (UNII: ZY81Z83H0X) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ) Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H) Propylene Carbonate (UNII: 8D08K3S51E) Dimethicone (UNII: 92RU3N3Y1O) Disteardimonium Hectorite (UNII: X687XDK09L) Sodium Chloride (UNII: 451W47IQ8X) Edetate Disodium (UNII: 7FLD91C86K) Caprylyl Glycol (UNII: 00YIU5438U) Phenoxyethanol (UNII: HIE492ZZ3T) Chlorphenesin (UNII: I670DAL4SZ) Ferric Oxide Red (UNII: 1K09F3G675) Ferric Oxide Yellow (UNII: EX438O2MRT) Ferrosoferric Oxide (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-1135-1 1 in 1 CARTON 10/27/2014 1 40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M020 10/27/2014 NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - PINK
octinoxate and octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-1138 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 28 mg in 1 mL Inactive Ingredients Ingredient Name Strength Hamamelis Virginiana Top Water (UNII: NT00Y05A2V) Cyclomethicone 5 (UNII: 0THT5PCI0R) Butylene Glycol (UNII: 3XUS85K0RA) Titanium Dioxide (UNII: 15FIX9V2JP) Cyclomethicone (UNII: NMQ347994Z) Cyclomethicone 6 (UNII: XHK3U310BA) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Hexyl Laurate (UNII: 4CG9F9W01Q) Polyglyceryl-4 Isostearate (UNII: 820DPX33S7) Aloe Vera Leaf (UNII: ZY81Z83H0X) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ) Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H) Propylene Carbonate (UNII: 8D08K3S51E) Dimethicone (UNII: 92RU3N3Y1O) Disteardimonium Hectorite (UNII: X687XDK09L) Sodium Chloride (UNII: 451W47IQ8X) Edetate Disodium (UNII: 7FLD91C86K) Caprylyl Glycol (UNII: 00YIU5438U) Phenoxyethanol (UNII: HIE492ZZ3T) Chlorphenesin (UNII: I670DAL4SZ) Ferric Oxide Red (UNII: 1K09F3G675) Ferric Oxide Yellow (UNII: EX438O2MRT) Ferrosoferric Oxide (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-1138-1 1 in 1 CARTON 10/27/2014 1 40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M020 10/27/2014 NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - PINK OCHRE
octinoxate and octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-1136 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 28 mg in 1 mL Inactive Ingredients Ingredient Name Strength Hamamelis Virginiana Top Water (UNII: NT00Y05A2V) Cyclomethicone 5 (UNII: 0THT5PCI0R) Butylene Glycol (UNII: 3XUS85K0RA) Titanium Dioxide (UNII: 15FIX9V2JP) Cyclomethicone (UNII: NMQ347994Z) Cyclomethicone 6 (UNII: XHK3U310BA) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Hexyl Laurate (UNII: 4CG9F9W01Q) Polyglyceryl-4 Isostearate (UNII: 820DPX33S7) Aloe Vera Leaf (UNII: ZY81Z83H0X) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ) Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H) Propylene Carbonate (UNII: 8D08K3S51E) Dimethicone (UNII: 92RU3N3Y1O) Disteardimonium Hectorite (UNII: X687XDK09L) Sodium Chloride (UNII: 451W47IQ8X) Edetate Disodium (UNII: 7FLD91C86K) Caprylyl Glycol (UNII: 00YIU5438U) Phenoxyethanol (UNII: HIE492ZZ3T) Chlorphenesin (UNII: I670DAL4SZ) Ferric Oxide Red (UNII: 1K09F3G675) Ferric Oxide Yellow (UNII: EX438O2MRT) Ferrosoferric Oxide (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-1136-1 1 in 1 CARTON 10/27/2014 1 40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M020 10/27/2014 NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - SAND
octinoxate and octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-1114 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 28 mg in 1 mL Inactive Ingredients Ingredient Name Strength Hamamelis Virginiana Top Water (UNII: NT00Y05A2V) Cyclomethicone 5 (UNII: 0THT5PCI0R) Butylene Glycol (UNII: 3XUS85K0RA) Titanium Dioxide (UNII: 15FIX9V2JP) Cyclomethicone (UNII: NMQ347994Z) Cyclomethicone 6 (UNII: XHK3U310BA) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Hexyl Laurate (UNII: 4CG9F9W01Q) Polyglyceryl-4 Isostearate (UNII: 820DPX33S7) Aloe Vera Leaf (UNII: ZY81Z83H0X) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ) Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H) Propylene Carbonate (UNII: 8D08K3S51E) Dimethicone (UNII: 92RU3N3Y1O) Disteardimonium Hectorite (UNII: X687XDK09L) Sodium Chloride (UNII: 451W47IQ8X) Edetate Disodium (UNII: 7FLD91C86K) Caprylyl Glycol (UNII: 00YIU5438U) Phenoxyethanol (UNII: HIE492ZZ3T) Chlorphenesin (UNII: I670DAL4SZ) Ferric Oxide Red (UNII: 1K09F3G675) Ferric Oxide Yellow (UNII: EX438O2MRT) Ferrosoferric Oxide (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-1114-1 1 in 1 CARTON 10/27/2014 1 40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M020 10/27/2014 Labeler - NSE Products, Inc. (803486393)
