Label: NU SKIN AGELOC ME DAY T9 BROAD SPECTRUM SPF 25- octinoxate, avobenzone, octocrylene, and homosalate lotion
- NDC Code(s): 62839-1637-1
- Packager: NSE Products, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 26, 2019
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
-
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
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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
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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
- Questions?
- PRINCIPAL DISPLAY PANEL - 28 ml Cartridge Carton
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INGREDIENTS AND APPEARANCE
NU SKIN AGELOC ME DAY T9 BROAD SPECTRUM SPF 25
octinoxate, avobenzone, octocrylene, and homosalate lotionProduct 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)
