AGELOC LUMISPA TREATMENT CLEANSER ACNE- salicylic acid lotion

ageLOC LumiSpa Treatment Cleanser Acne by

Drug Labeling and Warnings

ageLOC LumiSpa Treatment Cleanser Acne 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

Salicylic Acid (0.5%)

Purpose

Acne treatment

Uses

• For the treatment of acne.
• Penetrates pores to eliminate most acne blemishes.

Warnings

• For external use only.

• When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time unless directed by a doctor. If swallowed, get medical help or contact a Poison Control Center right away.

• Keep out of reach of children.

Directions

• For face.
• Dampen skin with warm water.
• Apply ample treatment cleanser evenly over face, avoiding eye area.
• For optimal results, use with ageLOC® LumiSpa™ device as directed in ageLOC LumiSpa User's Manual.

Inactive Ingredients

Water (Aqua), Cetearyl Alcohol, Glycerin, PEG-8 Dimethicone, Cocamidopropyl Betaine, Caprylyl/Capryl Glucoside, Capryl/Capramidopropyl Betaine, Carbomer, Narcissus Tazetta Bulb Extract, Epilobium Angustifolium Flower/Leaf/Stem Extract, Schizandra Chinensis Fruit Extract, Xanthan Gum, Carnosine, Oryza Sativa (Rice) Extract, Disodium EDTA, Phenoxyethanol, Hydroxyacetophenone, Sodium Hydroxide, Sodium Chloride.

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 100 ml Tube Label

NU SKIN®

ageLOC®

LumiSpa™

TREATMENT CLEANSER
acne

100 ml e (3.4 fl.oz.)

INGREDIENTS AND APPEARANCE

AGELOC LUMISPA TREATMENT CLEANSER ACNE 
salicylic acid lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-1495
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
Glycerin (UNII: PDC6A3C0OX)
PEG-8 Dimethicone (UNII: GIA7T764OD)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
Capryl/Capramidopropyl Betaine (UNII: 231H3ZT9NE)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
NARCISSUS TAZETTA BULB (UNII: K17762966S)
EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)
SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)
Xanthan Gum (UNII: TTV12P4NEE)
Carnosine (UNII: 8HO6PVN24W)
RICE GERM (UNII: 7N2B70SFEZ)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
Phenoxyethanol (UNII: HIE492ZZ3T)
Sodium Hydroxide (UNII: 55X04QC32I)
Sodium Chloride (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-1495-1	100 mL in 1 TUBE; Type 0: Not a Combination Product	10/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	10/01/2017

Labeler - NSE Products, Inc (803486393)