NDC | 62839-1345-1 |
Set ID | afd1ff5a-a9d0-4544-83f3-c4ddf87647f6 |
Category | HUMAN OTC DRUG LABEL |
Packager | NSE Products, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- 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 liberally 15 minutes before sun exposure.
- Reapply:
- After 40 minutes of swimming or sweating
- Immediately after towel drying
- At least every 2 hours
- Children under 6 months: Ask a doctor
-
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.
-
Inactive Ingredients
Acrylates Copolymer, Allantoin, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Bisabolol, Butylene Glycol, Caprylic/Capric Triglyceride, Carbomer, Caprylyl Glycol, Carthamus Tinctorius (Safflower) Seed Oil, Cetyl Alcohol, Chlorphenesin, Cyclohexasiloxane, Cyclopentasiloxane, Dimethicone/Vinyl Dimethicone Crosspolymer, Dimethicone/Vinyltrimethylsiloxysilicate Crosspolymer, Disodium EDTA, Fragrance (Parfum), Glyceryl Stearate, Haematococcus Pluvialis Extract, 1,2-Hexanediol, Panthenol, PEG-100 Stearate, Phenoxyethanol, Physalis Angulata Extract, Polyacrylate-13, Polyisobutene, Polysorbate 20, Steareth-2, Steareth-21, Titanium Dioxide, Tocopherol, Water (Aqua), Xanthan Gum.
- Other Information
- Questions?
- PRINCIPAL DISPLAY PANEL - 100 mL Bottle Carton
-
INGREDIENTS AND APPEARANCE
NU SKIN SUNRIGHT 50 BROAD SPECTRUM SPF 50
avobenzone, homosalate, octinoxate, octisalate, and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-1345 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 100 mg in 1 mL Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 75 mg in 1 mL Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 50 mg in 1 mL Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 65 mg in 1 mL Inactive Ingredients Ingredient Name Strength Allantoin (UNII: 344S277G0Z) Aloe Vera Leaf (UNII: ZY81Z83H0X) Aminomethylpropanol (UNII: LU49E6626Q) Levomenol (UNII: 24WE03BX2T) Butylene Glycol (UNII: 3XUS85K0RA) Medium-Chain Triglycerides (UNII: C9H2L21V7U) Caprylyl Glycol (UNII: 00YIU5438U) Safflower Oil (UNII: 65UEH262IS) Cetyl Alcohol (UNII: 936JST6JCN) Chlorphenesin (UNII: I670DAL4SZ) Cyclomethicone 6 (UNII: XHK3U310BA) Cyclomethicone 5 (UNII: 0THT5PCI0R) Edetate Disodium (UNII: 7FLD91C86K) Glyceryl Monostearate (UNII: 230OU9XXE4) Haematococcus Pluvialis (UNII: 31T0FF0472) 1,2-Hexanediol (UNII: TR046Y3K1G) Panthenol (UNII: WV9CM0O67Z) PEG-100 Stearate (UNII: YD01N1999R) Phenoxyethanol (UNII: HIE492ZZ3T) Physalis Angulata (UNII: W4TKW9D5GG) Steareth-2 (UNII: V56DFE46J5) Steareth-21 (UNII: 53J3F32P58) Polysorbate 20 (UNII: 7T1F30V5YH) Titanium Dioxide (UNII: 15FIX9V2JP) Tocopherol (UNII: R0ZB2556P8) Water (UNII: 059QF0KO0R) Xanthan Gum (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-1345-1 1 in 1 CARTON 06/02/2014 1 100 mL in 1 BOTTLE, PLASTIC; 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 06/02/2014 Labeler - NSE Products, Inc. (803486393)