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

Nu Skin by

Drug Labeling and Warnings

Nu Skin 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

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.
• Cover the entire face with a thin layer every morning after toner.
• If bothersome dryness or peeling occurs, reduce application to every other day.

Inactive Ingredients

Water (Aqua), Butylene Glycol, Methyl Pyrrolidone, Gluconolactone, Mandelic Acid, Sodium Hydroxide, Camellia Sinensis Leaf Extract,1 Glycerin, Sclerotium Gum, Arginine, Polyquaternium-10, Ethylene/Acrylic Acid Copolymer, Disodium EDTA, Chlorphenesin, Methylparaben.

1 White Tea

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 30 ml Carton

Nu Skin Clear Action®

Acne Medication Day Treatment

NU SKIN ®

30 ml e (1.0 fl. oz.)

INGREDIENTS AND APPEARANCE

NU SKIN  CLEAR ACTION ACNE MEDICATION DAY TREATMENT
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-1038
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 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
METHYLPYRROLIDONE (UNII: JR9CE63FPM)
Gluconolactone (UNII: WQ29KQ9POT)
Mandelic Acid (UNII: NH496X0UJX)
Sodium Hydroxide (UNII: 55X04QC32I)
Green Tea Leaf (UNII: W2ZU1RY8B0)
Glycerin (UNII: PDC6A3C0OX)
Arginine (UNII: 94ZLA3W45F)
Edetate Disodium (UNII: 7FLD91C86K)
Chlorphenesin (UNII: I670DAL4SZ)
Methylparaben (UNII: A2I8C7HI9T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-1038-9	1 in 1 CARTON	01/25/2002
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	01/25/2002

Labeler - NSE Products, Inc. (803486393)