NU SKIN AGELOC ME DAY T9 BROAD SPECTRUM SPF 25- octinoxate, avobenzone, octocrylene, and homosalate lotion

Nu Skin ageLOC Me Day T9 Broad Spectrum SPF 25 by

Drug Labeling and Warnings

Nu Skin ageLOC Me Day T9 Broad Spectrum SPF 25 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 Ingredient

Octinoxate (4.0%),
Avobenzone (2.3%),
Octocrylene (2.0%),
Homosalate (2.0%)

Purpose

Sunscreen

Uses

• Helps prevent sunburn.
• 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.

Warnings

• 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

• After applying serum and allowing it to dry, apply moisturizer in an upward, outward motion to the face and neck. If layering additional products, allow each to dry completely before applying the next.
• 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

Inactive Ingredients

Water (Aqua), Butylene Glycol, Isostearyl Alcohol, Isononyl Isononanoate, Dimethicone, Polymethyl Methacrylate, Butylene Glycol Cocoate, Diphenyl Dimethicone/Vinyl Diphenyl Dimethicone/Silsesquioxane Crosspolymer, Epilobium Angustifolium Flower/Leaf/Stem Extract, Glycerin, Camellia Sinensis Leaf Extract, Oryza Sativa (Rice) Extract, Plankton Extract, Narcissus Tazetta Bulb Extract, Dunaliella Salina Extract, Tocopherol, Bisabolol, Ethylcellulose, Sodium Dehydroacetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Schizandra Chinensis Fruit Extract, Corn Starch Modified, Hydroxyacetophenone, Squalane, PEG-40 Hydrogenated Castor Oil, Zea Mays (Corn) Oil, Caprylyl Methicone, 7-Dehydrocholesterol, Xanthan Gum, Disodium EDTA, Sodium Hydroxide, Fragrance (Parfum), Phenoxyethanol

Other Information

• Protect this product from excessive heat and direct sun.

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 28 ml Cartridge Carton

NU SKIN®

ageLOC me™ DAY T9 BROAD SPECTRUM SPF 25

28 ml e (0.95 fl. oz.)

INGREDIENTS AND APPEARANCE

NU SKIN AGELOC ME DAY T9 BROAD SPECTRUM SPF 25 
octinoxate, avobenzone, octocrylene, and homosalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-1637
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	40 mg  in 1 mL
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	23 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	20 mg  in 1 mL
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S)	Homosalate	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Isostearyl Alcohol (UNII: Q613OCQ44Y)
Isononyl Isononanoate (UNII: S4V5BS6GCX)
Dimethicone (UNII: 92RU3N3Y1O)
Phenoxyethanol (UNII: HIE492ZZ3T)
Caprylyl Trisiloxane (UNII: Q95M2P1KJL)
Squalane (UNII: GW89575KF9)
Glycerin (UNII: PDC6A3C0OX)
Rice Germ (UNII: 7N2B70SFEZ)
Polyoxyl 40 Hydrogenated Castor Oil (UNII: 7YC686GQ8F)
Xanthan Gum (UNII: TTV12P4NEE)
ETHYLCELLULOSE, UNSPECIFIED (UNII: 7Z8S9VYZ4B)
Levomenol (UNII: 24WE03BX2T)
Edetate Disodium (UNII: 7FLD91C86K)
Sodium Hydroxide (UNII: 55X04QC32I)
Sodium Dehydroacetate (UNII: 8W46YN971G)
Green Tea Leaf (UNII: W2ZU1RY8B0)
Schisandra Chinensis Fruit (UNII: ABS794681C)
Corn Oil (UNII: 8470G57WFM)
Epilobium Angustifolium Flowering Top (UNII: 08H094218D)
Dunaliella Salina (UNII: F4O1DKI9A6)
Narcissus Tazetta Bulb (UNII: K17762966S)
7-Dehydrocholesterol (UNII: BK1IU07GKF)
Tocopherol (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-1637-1	1 in 1 CARTON	05/01/2016
1		28 mL in 1 CARTRIDGE; 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	05/01/2016

Labeler - NSE Products, Inc. (803486393)