Label: AGELOC TRU FACE RADIANT DAY- avobenzone, homosalate, octisalate, and octocrylene lotion
- NDC Code(s): 62839-4268-1
- Packager: NSE Products, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 31, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
-
Use
- 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.
- Warnings
-
Directions
- Apply evenly to face and neck each morning as the final step in your skin care routine.
-
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 Broad Spectrum 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.
- 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), Glycerin, Cetyl Dimethicone, Cyclopentasiloxane, Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Caprylyl Glycol, Glyceryl Stearate, PEG-100 Stearate, Dimethicone, Cyclohexasiloxane, Dimethicone/Vinyl Dimethicone Crosspolymer, Cetyl Alcohol, Methyl Gluceth-10, Steareth-2, Steareth-21, Isohexadecane, Nylon-12, Hydrolyzed Jojoba Esters, Jojoba Esters, Bambusa Vulgaris Leaf/Stem Extract, Glucosamine HCl, Pisum Sativum (Pea) Extract, Hexapeptide-2, Narcissus Tazetta Bulb Extract, Schizandra Chinensis Fruit Extract, Butyrospermum Parkii (Shea Butter), Polysorbate 80, Titanium Dioxide, Butylene Glycol, Citric Acid, Disodium EDTA, Fragrance (Parfum), Chlorphenesin, Phenoxyethanol.
- Other Information
- Questions?
- PRINCIPAL DISPLAY PANEL - 30 mL Tube Carton
-
INGREDIENTS AND APPEARANCE
AGELOC TRU FACE RADIANT DAY
avobenzone, homosalate, octisalate, and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-4268 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone 30 mg in 1 mL Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S) Homosalate 50 mg in 1 mL Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 40 mg in 1 mL Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ACRYLAMIDE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (120000 MPA.S AT 1%) (UNII: 5F4963KLHS) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) Caprylyl Glycol (UNII: 00YIU5438U) PEG-100 MONOSTEARATE (UNII: YD01N1999R) Steareth-2 (UNII: V56DFE46J5) Steareth-21 (UNII: 53J3F32P58) Methyl Gluceth-10 (UNII: N0MWT4C7WH) Cetyl Alcohol (UNII: 936JST6JCN) Isohexadecane (UNII: 918X1OUF1E) DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O) Nylon-12 (UNII: 446U8J075B) CYCLOMETHICONE 6 (UNII: XHK3U310BA) Phenoxyethanol (UNII: HIE492ZZ3T) Chlorphenesin (UNII: I670DAL4SZ) HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W) Polysorbate 80 (UNII: 6OZP39ZG8H) GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY) Titanium Dioxide (UNII: 15FIX9V2JP) SHEA BUTTER (UNII: K49155WL9Y) PEA (UNII: W4X7H8GYFM) Butylene Glycol (UNII: 3XUS85K0RA) EDETATE DISODIUM (UNII: 7FLD91C86K) BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C) NARCISSUS TAZETTA BULB (UNII: K17762966S) Hexapeptide-2 (UNII: 4H7N4I6X6A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-4268-1 1 in 1 CARTON 05/01/2025 1 30 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M020 05/01/2025 Labeler - NSE Products, Inc. (803486393)

