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NDC 62839-3904-01 Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22 30; 50; 40; 20 mg/mL; mg/mL; mg/mL; mg/mL Details

Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22 30; 50; 40; 20 mg/mL; mg/mL; mg/mL; mg/mL

Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22 is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by NSE Products, Inc.. The primary component is AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE.

Product Information

NDC	62839-3904
Product ID	62839-3904_3cc7123b-dc30-47d9-97a4-96eb30f8cda7
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Nu Skin ageLOC Radiant Day Broad Spectrum SPF 22
Proprietary Name Suffix	n/a
Non-Proprietary Name	Avobenzone, Homosalate, Octisalate, and Octocrylene
Product Type	HUMAN OTC DRUG
Dosage Form	LOTION
Route	TOPICAL
Active Ingredient Strength	30; 50; 40; 20
Active Ingredient Units	mg/mL; mg/mL; mg/mL; mg/mL
Substance Name	AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Labeler Name	NSE Products, Inc.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part352
Listing Certified Through	2024-12-31

Package

Package Images

NDC 62839-3904-01 (62839390401)

Pricing Information	N/A
NDC Package Code	62839-3904-1
Billing NDC	62839390401
Package	1 TUBE, WITH APPLICATOR in 1 CARTON (62839-3904-1) / 25 mL in 1 TUBE, WITH APPLICATOR
Marketing Start Date	2013-05-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 649a9c28-bfd4-404c-90d5-5d0ea8c7b645 Details

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Avobenzone (3%), Homosalate (5%), Octisalate (4%), Octocrylene (2%)

Purpose

Sunscreen

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

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

Illuminate your skin each day. To complete your morning regimen, squeeze a pea-sized amount onto fingertips and apply in an upward, outward motion to face and neck. Avoid eye area.
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. –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

Protect this product from excessive heat and direct sun.

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 25 ml Tube Carton

ageLOC® RADIANT DAY

BROAD SPECTRUM SPF 22

NU SKIN®

25 ml e (0.85 fl .oz.)

PRINCIPAL DISPLAY PANEL - 25 ml Tube Carton

INGREDIENTS AND APPEARANCE

NU SKIN AGELOC RADIANT DAY BROAD SPECTRUM SPF 22

avobenzone, homosalate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62839-3904
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
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

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
CETYL ALCOHOL (UNII: 936JST6JCN)
METHYL GLUCETH-10 (UNII: N0MWT4C7WH)
STEARETH-2 (UNII: V56DFE46J5)
STEARETH-21 (UNII: 53J3F32P58)
ISOHEXADECANE (UNII: 918X1OUF1E)
DIMETHICONE (UNII: 92RU3N3Y1O)
NYLON-12 (UNII: 446U8J075B)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CHLORPHENESIN (UNII: I670DAL4SZ)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
SHEA BUTTER (UNII: K49155WL9Y)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
PEA (UNII: W4X7H8GYFM)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
EDETATE DISODIUM (UNII: 7FLD91C86K)
BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V)
NARCISSUS TAZETTA BULB (UNII: K17762966S)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:62839-3904-1	1 in 1 CARTON	05/01/2013
1		25 mL in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	05/01/2013

Labeler - NSE Products, Inc. (803486393)

Revised: 1/2022

Document Id: 3cc7123b-dc30-47d9-97a4-96eb30f8cda7

Set id: 649a9c28-bfd4-404c-90d5-5d0ea8c7b645

Version: 3

Effective Time: 20220111