Nu Skin Nu Colour

Manufacturer
NSE Products, Inc.
Effective date
2013-06-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:40:28

Label at a glance#

ProductNu Skin Nu Colour Tinted Moisturizer Broad Spectrum SPF 15 Beige
Active ingredientOctinoxate, Octisalate
Label structure13 sections

Indications and 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.

Dosage and administration

Shake well before use. Smooth over face and neck area blending well. Seal with powder if desired. Sunprotection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. –2p.m. Wear long-sleeved shirt...

Storage and handling

Protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate (5%), Octisalate (2%).

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

  • For external use only.

OTC - DO NOT USE SECTION

  • Do not use on damaged or broken skin

OTC - STOP USE SECTION

  • Stop use and ask a doctor if rash occurs

OTC - WHEN USING SECTION

  • When using this product, keep out of eyes. Rinse with water to remove.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Shake well before use. Smooth over face and neck area blending well. Seal with powder if desired.
  • Sunprotection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF of 15 or higher and other sun protection measures including:
    • Limit time in the sun, especially from 10 a.m. –2p.m.
    • Wear long-sleeved shirts, pants, hats, and sunglasses.
    • Apply liberally 15 minutes before sun exposure
    • Use a water resistant sunscreen if swimming or sweating
    • Reapply at least every 2 hours
    • Children under 6 months: Ask a doctor.

Other Information

STORAGE AND HANDLING SECTION

  • Protect this product from excessive heat and direct sun.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Hamamelis Virginiana (Witch Hazel) Water, Cyclopentasiloxane, Titanium Dioxide (Cl 77891), Cyclomethicone, Dimethicone Crosspolymer, Cyclohexasiloxane, Butylene Glycol, Phenyl Trimethicone, Nylon-12, Hexyl Laurate, Cetyl PEG/PPG-10/1 Dimethicone, Polyglyceryl-4 Isostearate, Sodium Chloride, Aloe Barbadensis Leaf Juice, Retinyl Palmitate, Tocopheryl Acetate, Tetrahexyldecyl Ascorbate, Zea Mays (Corn) Oil, Methicone, Dimethicone, Disteardimonium Hectorite, Propylene Carbonate, Disodium EDTA, Fragrance, Phenoxyethanol, Methylparaben, Propylparaben.

May Contain

SPL UNCLASSIFIED SECTION

Iron Oxides (CI 77491, CI 77492, CI 77499), Chromium Oxide Greens (CI 77288).

Questions?

OTC - QUESTIONS SECTION

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton (Beige)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Nu Colour®

Tinted Moisturizer

Broad Spectrum
SPF 15

NU SKIN®

40 ml e (1.4 fl.oz.)

Principal Display Panel - 40 ml Bottle Carton (Beige)
Principal Display Panel - 40 ml Bottle Carton (Beige)

PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton (Fair)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Nu Colour®

Tinted Moisturizer

Broad Spectrum
SPF 15

NU SKIN®

40 ml e (1.4 fl.oz.)

Principal Display Panel - 40 ml Bottle Carton (Fair)
Principal Display Panel - 40 ml Bottle Carton (Fair)

PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton (Honey)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Nu Colour®

Tinted Moisturizer

Broad Spectrum
SPF 15

NU SKIN®

40 ml e (1.4 fl.oz.)

Principal Display Panel - 40 ml Bottle Carton (Honey)
Principal Display Panel - 40 ml Bottle Carton (Honey)

PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton (Sand)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Nu Colour®

Tinted Moisturizer

Broad Spectrum
SPF 15

NU SKIN®

40 ml e (1.4 fl.oz.)

Principal Display Panel - 40 ml Bottle Carton (Sand)
Principal Display Panel - 40 ml Bottle Carton (Sand)

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62839-1101NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 BEIGE (OCTINOXATE AND OCTISALATE) LOTION NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 FAIR (OCTINOXATE AND OCTISALATE) LOTION NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 HONEY (OCTINOXATE AND OCTISALATE) LOTION NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 SAND (OCTINOXATE AND OCTISALATE) LOTION [NSE PRODUCTS, INC.]2Legacy NDC20130625_55f79a4b-1654-41f7-b456-50ffdcaae845.zip
62839-1102NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 BEIGE (OCTINOXATE AND OCTISALATE) LOTION NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 FAIR (OCTINOXATE AND OCTISALATE) LOTION NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 HONEY (OCTINOXATE AND OCTISALATE) LOTION NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 SAND (OCTINOXATE AND OCTISALATE) LOTION [NSE PRODUCTS, INC.]2Legacy NDC20130625_55f79a4b-1654-41f7-b456-50ffdcaae845.zip
62839-1103NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 BEIGE (OCTINOXATE AND OCTISALATE) LOTION NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 FAIR (OCTINOXATE AND OCTISALATE) LOTION NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 HONEY (OCTINOXATE AND OCTISALATE) LOTION NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 SAND (OCTINOXATE AND OCTISALATE) LOTION [NSE PRODUCTS, INC.]2Legacy NDC20130625_55f79a4b-1654-41f7-b456-50ffdcaae845.zip
62839-1104NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 BEIGE (OCTINOXATE AND OCTISALATE) LOTION NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 FAIR (OCTINOXATE AND OCTISALATE) LOTION NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 HONEY (OCTINOXATE AND OCTISALATE) LOTION NU SKIN NU COLOUR TINTED MOISTURIZER BROAD SPECTRUM SPF 15 SAND (OCTINOXATE AND OCTISALATE) LOTION [NSE PRODUCTS, INC.]2Legacy NDC20130625_55f79a4b-1654-41f7-b456-50ffdcaae845.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OctinoxateACTIVE INGREDIENT4Y5P7MUD512
OctisalateACTIVE INGREDIENT4X49Y0596W2
OctinoxateACTIVE MOIETY4Y5P7MUD512
OctisalateACTIVE MOIETY4X49Y0596W2
.Alpha.-Tocopherol AcetateINACTIVE INGREDIENT9E8X80D2L02
Aloe Vera LeafINACTIVE INGREDIENTZY81Z83H0X2
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA2
Chromic OxideINACTIVE INGREDIENTX5Z09SU8592
Corn OilINACTIVE INGREDIENT8470G57WFM2
CyclomethiconeINACTIVE INGREDIENTNMQ347994Z2
Cyclomethicone 5INACTIVE INGREDIENT0THT5PCI0R2
Cyclomethicone 6INACTIVE INGREDIENTXHK3U310BA2
DimethiconeINACTIVE INGREDIENT92RU3N3Y1O2
Disteardimonium HectoriteINACTIVE INGREDIENTX687XDK09L2
Edetate DisodiumINACTIVE INGREDIENT7FLD91C86K2
Ferric Oxide RedINACTIVE INGREDIENT1K09F3G6752
Ferric Oxide YellowINACTIVE INGREDIENTEX438O2MRT2
Ferrosoferric OxideINACTIVE INGREDIENTXM0M87F3572
Hamamelis Virginiana Top WaterINACTIVE INGREDIENTNT00Y05A2V2
Hexyl LaurateINACTIVE INGREDIENT4CG9F9W01Q2
MethylparabenINACTIVE INGREDIENTA2I8C7HI9T2
Nylon-12INACTIVE INGREDIENT446U8J075B2
PhenoxyethanolINACTIVE INGREDIENTHIE492ZZ3T2
Phenyl TrimethiconeINACTIVE INGREDIENTDR0K5NOJ4R2
Polyglyceryl-4 IsostearateINACTIVE INGREDIENT820DPX33S72
Propylene CarbonateINACTIVE INGREDIENT8D08K3S51E2
PropylparabenINACTIVE INGREDIENTZ8IX2SC1OH2
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8X2
Tetrahexyldecyl AscorbateINACTIVE INGREDIENT9LBV3F07AZ2
Titanium DioxideINACTIVE INGREDIENT15FIX9V2JP2
Vitamin A PalmitateINACTIVE INGREDIENT1D1K0N0VVC2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 3 · 116 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 8 · 480 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSUSPENSION/ DROPS / AURICULAR (OTIC)3 mgExact identifier — unii candidate
134 equally ranked IID candidates
PropylparabenPROPYLPARABENZ8IX2SC1OHCONCENTRATE / ORAL2.5 mg/5mlExact identifier — unii candidate
68 equally ranked IID candidates
Ferrosoferric OxideFERROSOFERRIC OXIDEXM0M87F357TABLET, DELAYED RELEASE / ORAL6 mgExact identifier — unii candidate
10 equally ranked IID candidates
Ferric Oxide RedFERRIC OXIDE RED1K09F3G675TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL0.15 mgExact identifier — unii candidate
21 equally ranked IID candidates
PropylparabenPROPYLPARABENZ8IX2SC1OHSOLUTION/ DROPS / OPHTHALMIC0.01 %w/vExact identifier — unii candidate
68 equally ranked IID candidates
PropylparabenPROPYLPARABENZ8IX2SC1OHSOLUTION / OPHTHALMIC0.02 %w/wExact identifier — unii candidate
68 equally ranked IID candidates
PropylparabenPROPYLPARABENZ8IX2SC1OHINJECTION, SUSPENSION / SUBCUTANEOUS0.02 %w/vExact identifier — unii candidate
68 equally ranked IID candidates
MethylparabenMETHYLPARABENA2I8C7HI9TSOLUTION / RESPIRATORY (INHALATION)0.03 %w/wExact identifier — unii candidate
79 equally ranked IID candidates
MethylparabenMETHYLPARABENA2I8C7HI9TINJECTION, SOLUTION / INTRAVENOUS45 mgExact identifier — unii candidate
79 equally ranked IID candidates
Edetate DisodiumEDETATE DISODIUM7FLD91C86KSOLUTION / ORAL432 mgExact identifier — unii candidate
77 equally ranked IID candidates
Edetate DisodiumEDETATE DISODIUM7FLD91C86KSOLUTION / RESPIRATORY (INHALATION)43 mgExact identifier — unii candidate
77 equally ranked IID candidates
Edetate DisodiumEDETATE DISODIUM7FLD91C86KLIQUID / INTRAVENOUS0.03 %w/vExact identifier — unii candidate
77 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INTRASYNOVIAL0.9 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
Edetate DisodiumEDETATE DISODIUM7FLD91C86KINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS19 mgExact identifier — unii candidate
77 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION / PARENTERAL210 mgExact identifier — unii candidate
134 equally ranked IID candidates
MethylparabenMETHYLPARABENA2I8C7HI9TINJECTION, SOLUTION / EPIDURAL30 mgExact identifier — unii candidate
79 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XTABLET, FILM COATED / ORAL100 mgExact identifier — unii candidate
134 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INTRACARDIAC70 mgExact identifier — unii candidate
134 equally ranked IID candidates
MethylparabenMETHYLPARABENA2I8C7HI9TGEL / VAGINAL8 mgExact identifier — unii candidate
79 equally ranked IID candidates
MethylparabenMETHYLPARABENA2I8C7HI9TSOLUTION / RECTAL0.13 %w/vExact identifier — unii candidate
79 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSPRAY / NASAL30 mgExact identifier — unii candidate
134 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, SUSPENSION, EXTENDED RELEASE / INTRAMUSCULAR24 mgExact identifier — unii candidate
134 equally ranked IID candidates
Ferrosoferric OxideFERROSOFERRIC OXIDEXM0M87F357CAPSULE, EXTENDED RELEASE / ORAL1.49 mgExact identifier — unii candidate
10 equally ranked IID candidates
PropylparabenPROPYLPARABENZ8IX2SC1OHSOLUTION, CONCENTRATE / ORAL0.2 mg/1mlExact identifier — unii candidate
68 equally ranked IID candidates
PropylparabenPROPYLPARABENZ8IX2SC1OHEMULSION / TOPICAL0.06 %w/wExact identifier — unii candidate
68 equally ranked IID candidates
CyclomethiconeCYCLOMETHICONENMQ347994ZLOTION / TOPICAL3510 mgExact identifier — unii candidate
5 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSUSPENSION / ORAL1126 mgExact identifier — unii candidate
134 equally ranked IID candidates
Edetate DisodiumEDETATE DISODIUM7FLD91C86KSHAMPOO / TOPICAL1 %w/wExact identifier — unii candidate
77 equally ranked IID candidates
MethylparabenMETHYLPARABENA2I8C7HI9TSOLUTION / ORAL346 mgExact identifier — unii candidate
79 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XPOWDER, DENTIFRICE / DENTAL0.03 mg/mgExact identifier — unii candidate
134 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, SUSPENSION / INTRA-ARTICULAR26 mgExact identifier — unii candidate
134 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XGEL / VAGINAL10 %w/wExact identifier — unii candidate
134 equally ranked IID candidates
Edetate DisodiumEDETATE DISODIUM7FLD91C86KINJECTION, SOLUTION / INTRAVENOUS7 mgExact identifier — unii candidate
77 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TCREAM / TOPICAL57 mgExact identifier — unii candidate
6 equally ranked IID candidates
Edetate DisodiumEDETATE DISODIUM7FLD91C86KEMULSION / TOPICAL0.11 %w/wExact identifier — unii candidate
77 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XCREAM / TOPICAL0.4 %w/wExact identifier — unii candidate
134 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XJELLY / NASALNAExact identifier — unii candidate
134 equally ranked IID candidates
MethylparabenMETHYLPARABENA2I8C7HI9TINJECTION / SUBCUTANEOUS22 mgExact identifier — unii candidate
79 equally ranked IID candidates
PropylparabenPROPYLPARABENZ8IX2SC1OHINJECTION, POWDER, FOR SOLUTION / INTRAMUSCULAR0.4 mgExact identifier — unii candidate
68 equally ranked IID candidates
MethylparabenMETHYLPARABENA2I8C7HI9TDROPS / AURICULAR (OTIC)0.01 %w/wExact identifier — unii candidate
79 equally ranked IID candidates
Ferric Oxide YellowFERRIC OXIDE YELLOWEX438O2MRTGRANULE, FOR SUSPENSION / ORAL11 mgExact identifier — unii candidate
20 equally ranked IID candidates
Titanium DioxideTITANIUM DIOXIDE15FIX9V2JPTABLET, DELAYED RELEASE / ORAL66 mgExact identifier — unii candidate
40 equally ranked IID candidates
Titanium DioxideTITANIUM DIOXIDE15FIX9V2JPCAPSULE, DELAYED RELEASE PELLETS / ORAL24 mgExact identifier — unii candidate
40 equally ranked IID candidates
Edetate DisodiumEDETATE DISODIUM7FLD91C86KSYRUP / ORAL40 mgExact identifier — unii candidate
77 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION / INTRAVASCULARNAExact identifier — unii candidate
134 equally ranked IID candidates
Ferric Oxide RedFERRIC OXIDE RED1K09F3G675TABLET, DELAYED RELEASE / ORAL37 mgExact identifier — unii candidate
21 equally ranked IID candidates
PropylparabenPROPYLPARABENZ8IX2SC1OHSPRAY / TOPICAL0.8 %w/wExact identifier — unii candidate
68 equally ranked IID candidates
PropylparabenPROPYLPARABENZ8IX2SC1OHSUSPENSION / SUBCUTANEOUS0.02 %w/vExact identifier — unii candidate
68 equally ranked IID candidates
Edetate DisodiumEDETATE DISODIUM7FLD91C86KENEMA / RECTAL60 mgExact identifier — unii candidate
77 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INFILTRATION648 mgExact identifier — unii candidate
134 equally ranked IID candidates
PropylparabenPROPYLPARABENZ8IX2SC1OHCAPSULE, EXTENDED RELEASE / ORAL0.22 mgExact identifier — unii candidate
68 equally ranked IID candidates
.Alpha.-Tocopherol Acetate.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0TABLET / ORAL0.5 mgExact identifier — unii candidate
3 equally ranked IID candidates
MethylparabenMETHYLPARABENA2I8C7HI9TINJECTION / EPIDURAL1 mgExact identifier — unii candidate
79 equally ranked IID candidates
MethylparabenMETHYLPARABENA2I8C7HI9TSOLUTION / NASAL250 mgExact identifier — unii candidate
79 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TLOTION / TOPICAL1 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
PropylparabenPROPYLPARABENZ8IX2SC1OHSOLUTION / RESPIRATORY (INHALATION)0.01 %w/wExact identifier — unii candidate
68 equally ranked IID candidates
MethylparabenMETHYLPARABENA2I8C7HI9TSOLUTION / INTRAMUSCULAR0.13 %w/vExact identifier — unii candidate
79 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XPOWDER, FOR SUSPENSION / ORAL98 mgExact identifier — unii candidate
134 equally ranked IID candidates
Ferric Oxide RedFERRIC OXIDE RED1K09F3G675LOTION / TOPICALNAExact identifier — unii candidate
21 equally ranked IID candidates
Ferric Oxide RedFERRIC OXIDE RED1K09F3G675CREAM / TOPICALNAExact identifier — unii candidate
21 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
fd4d2ced-c196-4b9b-a2fb-9cc953947b5255f79a4b-1654-41f7-b456-50ffdcaae8452026-03-31WarningsExact identifier
spl set id: 55f79a4b-1654-41f7-b456-50ffdcaae845

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.