NU SKIN AGELOC ME DAY S1 BROAD SPECTRUM SPF 25- homosalate, octinoxate, avobenzone, and octocrylene lotion

Nu Skin ageLOC Me Day S1 Broad Spectrum SPF 25 by

Drug Labeling and Warnings

Nu Skin ageLOC Me Day S1 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

Homosalate (4.0%),
Octinoxate (3.5%),
Avobenzone (3.0%),
Octocrylene (2.79%)

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, Caprylyl Methicone, Nylon-6/12, Octyldodecyl Neopentanoate, Glycerin, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Oryza Sativa (Rice) Extract, Methoxy PEG/PPG-25/4 Dimethicone, Hydrogenated Phosphatidylcholine, Caprylic/Capric Triglyceride, 4-t-Butylcyclohexanol, Hydroxyacetophenone, Polyisobutene, Schizandra Chinensis Fruit Extract, Camellia Sinensis Leaf Extract, Allantoin, Pentylene Glycol, 7-Dehydrocholesterol, Paeonia Lactiflora Extract, Epilobium Angustifolium Flower/Leaf/Stem Extract, Tocopherol, Narcissus Tazetta Bulb Extract, PEG-7 Trimethylolpropane Coconut Ether, Sorbitan Isostearate, Hydroxyphenyl Propamidobenzoic Acid, Bis-PEG/PPG-20/5 PEG/PPG-20/5 Dimethicone, Zea Mays (Corn) Oil, Xanthan Gum, Aminomethyl Propanol, Disodium EDTA, Chlorphenesin

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 S1 BROAD SPECTRUM SPF 25

28 ml e (0.95 fl . oz.)

INGREDIENTS AND APPEARANCE

NU SKIN AGELOC ME DAY S1 BROAD SPECTRUM SPF 25 
homosalate, octinoxate, avobenzone, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-1617
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S)	Homosalate	40 mg  in 1 mL
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	35 mg  in 1 mL
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	30 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	27.9 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Octyldodecyl Neopentanoate (UNII: X8725R883T)
Caprylyl Trisiloxane (UNII: Q95M2P1KJL)
Pentylene Glycol (UNII: 50C1307PZG)
Glycerin (UNII: PDC6A3C0OX)
Medium-Chain Triglycerides (UNII: C9H2L21V7U)
Rice Germ (UNII: 7N2B70SFEZ)
Xanthan Gum (UNII: TTV12P4NEE)
4-tert-Butylcyclohexanol (UNII: K0H1405S9C)
Chlorphenesin (UNII: I670DAL4SZ)
Allantoin (UNII: 344S277G0Z)
Edetate Disodium (UNII: 7FLD91C86K)
Epilobium Angustifolium Flowering Top (UNII: 08H094218D)
Green Tea Leaf (UNII: W2ZU1RY8B0)
Sorbitan Isostearate (UNII: 01S2G2C1E4)
Hydroxyphenyl Propamidobenzoic Acid (UNII: 25KRT26H77)
Schisandra Chinensis Fruit (UNII: ABS794681C)
Corn Oil (UNII: 8470G57WFM)
Narcissus Tazetta Bulb (UNII: K17762966S)
7-Dehydrocholesterol (UNII: BK1IU07GKF)
Aminomethylpropanol (UNII: LU49E6626Q)
Tocopherol (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-1617-1	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)