NU SKIN CLEAR ACTION ACNE MEDICATION NIGHT TREATMENT- salicylic acid gel

Nu Skin Clear Action Acne Medication Night Treatment by

Drug Labeling and Warnings

Nu Skin Clear Action Acne Medication Night Treatment 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 (0.55%)

Purpose

Acne treatment

Use

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

Warnings

• For external use only. Using other topical acne medication at the same time or immediately following the use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

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

Directions

• Cleanse the skin thoroughly before applying medication.
• Cover the entire affected area with a thin layer once daily.
• If bothersome dryness or peeling occurs, reduce application to every other day.
• Use at night following toner.
• Dispense about a dime size and apply lightly in an upward, outward motion to face and neck.

Inactive ingredients

Water (Aqua), Butylene Glycol, Methyl Gluceth-20, Polyacrylate-13, Ethoxydiglycol, Polyisobutene, Caprylyl Glycol, Glycerin, Fragrance (Parfum), Thioctic Acid,1 Tocopheryl Acetate, Phenoxyethanol, Chlorphenesin, Polysorbate 20, Sodium Hydroxide, Cyclodextrin, Tocopherol, Retinol, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Phytosphingosine, Tetrasodium EDTA, Citric Acid

1 Alpha Lipoic Acid

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 30 ml Tube Carton

Nu Skin Clear Action®
Acne Medication Night Treatment

NU SKIN®

30 ml e (1.0 fl. oz.)

INGREDIENTS AND APPEARANCE

NU SKIN CLEAR ACTION ACNE MEDICATION NIGHT TREATMENT 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-4731
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	5.5 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Methyl Gluceth-20 (UNII: J3QD0LD11P)
Diethylene Glycol Monoethyl Ether (UNII: A1A1I8X02B)
Caprylyl Glycol (UNII: 00YIU5438U)
Glycerin (UNII: PDC6A3C0OX)
Thioctic Acid (UNII: 73Y7P0K73Y)
Phenoxyethanol (UNII: HIE492ZZ3T)
Chlorphenesin (UNII: I670DAL4SZ)
Polysorbate 20 (UNII: 7T1F30V5YH)
Sodium Hydroxide (UNII: 55X04QC32I)
Tocopherol (UNII: R0ZB2556P8)
Retinol (UNII: G2SH0XKK91)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
Licorice (UNII: 61ZBX54883)
Phytosphingosine (UNII: GIN46U9Q2Q)
Edetate Sodium (UNII: MP1J8420LU)
Citric Acid Monohydrate (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-4731-1	1 in 1 CARTON	02/01/2013
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 FINAL	part333D	02/01/2013

Labeler - NSE Products, Inc (803486393)