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
- Marketing Status: OTC monograph 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 January 13, 2022
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.
-
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 FINAL part352 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 FINAL part352 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 FINAL part352 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 FINAL part352 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 FINAL part352 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 FINAL part352 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 FINAL part352 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 FINAL part352 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 FINAL part352 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 FINAL part352 10/27/2014 Labeler - NSE Products, Inc. (803486393)