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
NSE Products, Inc

----------

Nu Skin® Nu Colour® advanced tinted moisturizer broad spectrum SPF 15

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.
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

Protect this product from excessive heat and direct sun.

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 - Sand

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62839-1116
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	28 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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, UNSPECIFIED (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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62839-1116-1	1 in 1 CARTON	10/27/2014	11/01/2023
1		40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH DRUG	M020	10/27/2014	11/01/2023

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62839-1113
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	28 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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, UNSPECIFIED (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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62839-1113-1	1 in 1 CARTON	10/27/2014	01/01/2024
1		40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH DRUG	M020	10/27/2014	01/01/2024

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62839-1115
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	28 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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, UNSPECIFIED (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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62839-1115-1	1 in 1 CARTON	10/27/2014	12/01/2023
1		40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH DRUG	M020	10/27/2014	12/01/2023

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62839-1140
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	28 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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, UNSPECIFIED (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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62839-1140-1	1 in 1 CARTON	10/27/2014	12/01/2020
1		40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH DRUG	M020	10/27/2014	12/01/2020

NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - MEDIUM OCHRE
octinoxate and octisalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62839-1137
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	28 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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, UNSPECIFIED (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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62839-1137-1	1 in 1 CARTON	10/27/2014	01/01/2021
1		40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH DRUG	M020	10/27/2014	01/01/2021

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62839-1139
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	28 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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, UNSPECIFIED (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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62839-1139-1	1 in 1 CARTON	10/27/2014	02/01/2024
1		40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH DRUG	M020	10/27/2014	02/01/2024

NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - OCHRE
octinoxate and octisalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62839-1135
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	28 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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, UNSPECIFIED (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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62839-1135-1	1 in 1 CARTON	10/27/2014	01/01/2021
1		40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH DRUG	M020	10/27/2014	01/01/2021

NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - PINK
octinoxate and octisalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62839-1138
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	28 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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, UNSPECIFIED (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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62839-1138-1	1 in 1 CARTON	10/27/2014	01/01/2021
1		40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH DRUG	M020	10/27/2014	01/01/2021

NU SKIN NU COLOUR ADVANCED TINTED MOISTURIZER BROAD SPECTRUM SPF 15 - PINK OCHRE
octinoxate and octisalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62839-1136
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	28 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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, UNSPECIFIED (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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62839-1136-1	1 in 1 CARTON	10/27/2014	01/01/2024
1		40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH DRUG	M020	10/27/2014	01/01/2024

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62839-1114
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	28 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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, UNSPECIFIED (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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62839-1114-1	1 in 1 CARTON	10/27/2014	12/01/2023
1		40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH DRUG	M020	10/27/2014	12/01/2023

Labeler - NSE Products, Inc (803486393)

Revised: 3/2026

Document Id: a5efb5ce-7c5d-4a05-a0aa-1f0b0ad03a76

Set id: 22ea0f58-b79a-4813-9ccb-cb2d90aa9429

Version: 5

Effective Time: 20260331

NSE Products, Inc