NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - ALMOND- octinoxate, octisalate, and octocrylene lotion NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - BEIGE- octinoxate, octisalate, and octocrylene lotion NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - DELICATE IVORY- octinoxate, octisalate, and octocrylene lotion NU .......ne) lotion NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - SUNNY BEIGE- octinoxate, octisalate, and octocrylene lotion NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - SUNSET BEIGE- octinoxate, octisalate, and octocrylene lotion NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - TAWNY- octinoxate, octisalate, and octocrylene lotion

Nu Skin Nu Colour advanced finish broad spectrum SPF 15 - Tawny by

Drug Labeling and Warnings

Nu Skin Nu Colour advanced finish broad spectrum SPF 15 - Tawny by is a Otc medication manufactured, distributed, or labeled by NSE Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

Octinoxate 7.5%, Octisalate 2%, Octocrylene 4%.

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 broadspectrum 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.

Other Information

• Protect this product from excessive heat and direct sun.
• Use a water resistant sunscreen if swimming or sweating.
• Reapply at least every two hours.
• Children under 6 months: Ask a doctor.

Other Ingredients

Water (Aqua), Butylene Glycol, C12-15 Alkyl Benzoate, Glycerin, Isostearic Acid, Glyceryl Stearate, Stearic Acid, Cetyl Alcohol, Aloe Barbadensis Leaf Juice, Sodium Hyaluronate, Sodium PCA, Panthenol, Bisabolol, Morus Alba Root Extract, Squalane, Tocopheryl Acetate, Jojoba Esters, Tocopherol, Glycine Soja (Soybean) Oil, Nylon-12 Fluorescent Brightener 230 Salt, Dipalmitoyl Hydroxyproline, Niacinamide, Dimethicone, Magnesium Aluminum Silicate, Sodium C14-16 Olefin Sulfonate, Xanthan Gum, Polyvinylalcohol Crosspolymer, Sodium Dehydroacetate, Aminomethyl Propanol, Caprylyl Glycol, Phenoxyethanol.

May Contain

Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, CI 77492, CI 77499).

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Almond

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Beige

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Delicate Ivory

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Honey Beige

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Medium Beige

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Medium Ochre

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Mocha

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Neutral Beige

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Ochre

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Pink

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Pink Ochre

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Soft Beige

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Sunny Beige

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Sunset Beige

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - Tawny

NU SKIN®

Nu Colour®

advanced
liquid finish

broad spectrum
SPF 15

30 ml e (1.0 fl. oz.)

INGREDIENTS AND APPEARANCE

NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - ALMOND 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0857
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0857-1	1 in 1 CARTON	10/27/2014
1		30 mL in 1 BOTTLE, GLASS; 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 FINISH BROAD SPECTRUM SPF 15 - BEIGE 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0862
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0862-1	1 in 1 CARTON	08/01/2016
1		30 mL in 1 BOTTLE, GLASS; 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	08/01/2016

NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - DELICATE IVORY 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0855
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0855-1	1 in 1 CARTON	08/01/2016
1		30 mL in 1 BOTTLE, GLASS; 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	08/01/2016

NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - HONEY BEIGE 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0861
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0861-1	1 in 1 CARTON	08/01/2016
1		30 mL in 1 BOTTLE, GLASS; 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	08/01/2016

NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - MEDIUM BEIGE 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0867
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0867-1	1 in 1 CARTON	10/27/2014
1		30 mL in 1 BOTTLE, GLASS; 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 FINISH BROAD SPECTRUM SPF 15 - MEDIUM OCHRE 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0866
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0866-1	1 in 1 CARTON	10/27/2014
1		30 mL in 1 BOTTLE, GLASS; 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 FINISH BROAD SPECTRUM SPF 15 - MOCHA 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0860
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Glycerin (UNII: PDC6A3C0OX)
Titanium Dioxide (UNII: 15FIX9V2JP)
Isostearic Acid (UNII: X33R8U0062)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0860-1	1 in 1 CARTON	08/01/2016
1		30 mL in 1 BOTTLE, GLASS; 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	08/01/2016

NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - NEUTRAL BEIGE 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0853
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0853-1	1 in 1 CARTON	08/01/2016
1		30 mL in 1 BOTTLE, GLASS; 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	08/01/2016

NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - OCHRE 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0863
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0863-1	1 in 1 CARTON	10/27/2014
1		30 mL in 1 BOTTLE, GLASS; 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 FINISH BROAD SPECTRUM SPF 15 - PINK 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0864
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0864-1	1 in 1 CARTON	10/27/2014
1		30 mL in 1 BOTTLE, GLASS; 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 FINISH BROAD SPECTRUM SPF 15 - PINK OCHRE 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0865
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0865-1	1 in 1 CARTON	10/27/2014
1		30 mL in 1 BOTTLE, GLASS; 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 FINISH BROAD SPECTRUM SPF 15 - SOFT BEIGE 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0854
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0854-1	1 in 1 CARTON	10/27/2014
1		30 mL in 1 BOTTLE, GLASS; 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 FINISH BROAD SPECTRUM SPF 15 - SUNNY BEIGE 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0856
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0856-1	1 in 1 CARTON	10/27/2014
1		30 mL in 1 BOTTLE, GLASS; 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 FINISH BROAD SPECTRUM SPF 15 - SUNSET BEIGE 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0858
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Titanium Dioxide (UNII: 15FIX9V2JP)
Glycerin (UNII: PDC6A3C0OX)
Isostearic Acid (UNII: X33R8U0062)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0858-1	1 in 1 CARTON	08/01/2016
1		30 mL in 1 BOTTLE, GLASS; 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	08/01/2016

NU SKIN NU COLOUR ADVANCED FINISH BROAD SPECTRUM SPF 15 - TAWNY 
octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0859
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	20 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Glycerin (UNII: PDC6A3C0OX)
Titanium Dioxide (UNII: 15FIX9V2JP)
Isostearic Acid (UNII: X33R8U0062)
Ferric Oxide Yellow (UNII: EX438O2MRT)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Stearic Acid (UNII: 4ELV7Z65AP)
Cetyl Alcohol (UNII: 936JST6JCN)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Panthenol (UNII: WV9CM0O67Z)
Levomenol (UNII: 24WE03BX2T)
Morus Alba Root (UNII: CST1G9BZGD)
Squalane (UNII: GW89575KF9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Tocopherol (UNII: R0ZB2556P8)
Soybean Oil (UNII: 241ATL177A)
Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H)
Niacinamide (UNII: 25X51I8RD4)
Dimethicone (UNII: 92RU3N3Y1O)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Aminomethylpropanol (UNII: LU49E6626Q)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ferric Oxide Red (UNII: 1K09F3G675)
Ferrosoferric Oxide (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0859-1	1 in 1 CARTON	10/27/2014
1		30 mL in 1 BOTTLE, GLASS; 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)