AGELOC LUMISPA BLEMISH SERUM- salicylic acid lotion

Drug Labeling and Warnings

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

Salicylic Acid (2.0%)

Purpose

Acne Treatment

Uses

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

Warning

• For external use only.

• Do not use on damaged or broken skin.

• Stop use and ask a doctor if irritation occurs, only use one topical acne medication at a time unless directed by a doctor.

• When using this product, skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time.

• Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Cleanse the skin thoroughly before applying this product.
• Cover the entire affected area with a thin layer one to three times daily.
• Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a physician.
• If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Inactive Ingredients

Water (Aqua), Glycerin, Potassium Azeloyl Diglycinate, Propanediol, Dimethicone, Polyacrylate Crosspolymer-6, Silver, Morinda Citrifolia Extract, Narcissus Tazetta Bulb Extract, Schizandra Chinensis Fruit Extract, Dimethicone Crosspolymer, Hydrogenated Lecithin, Polyphosphorylcholine Glycol Acrylate, Butylene Glycol, Sodium Polyacrylate, Potassium Chloride, Ethylhexylglycerin, Phenoxyethanol, Sodium Benzoate, Citric Acid, Sodium Hydroxide.

Questions?

1-800-487-1000

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton

ageLOC®

LumiSpa®

BLEMISH SERUM

30 mL

INGREDIENTS AND APPEARANCE

AGELOC LUMISPA BLEMISH SERUM 
salicylic acid lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-2539
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Potassium Azeloyl Diglycinate (UNII: N02RVN6NYP)
Propanediol (UNII: 5965N8W85T)
DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
DIMETHICONE CROSSPOLYMER (450000 MPA.S) (UNII: UF7620L1W6)
Phenoxyethanol (UNII: HIE492ZZ3T)
Sodium Hydroxide (UNII: 55X04QC32I)
Butylene Glycol (UNII: 3XUS85K0RA)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
Silver (UNII: 3M4G523W1G)
Sodium Benzoate (UNII: OJ245FE5EU)
Ethylhexylglycerin (UNII: 147D247K3P)
Potassium Chloride (UNII: 660YQ98I10)
SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)
NARCISSUS TAZETTA BULB (UNII: K17762966S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-2539-1	1 in 1 CARTON	06/01/2023
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	M006	06/01/2023

Labeler - NSE Products, Inc. (803486393)