NU SKIN ANTIBACTERIAL BODY CLEANSING- triclosan 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 Ingredients

Triclosan (0.55%)

Purpose

Antimicrobial

Uses

• Offers multiple skin beneficial ingredients.
• Triclosan effectively fights infection causing germs and bacteria, while eliminating odor.
• Aloe vera and other soothing, conditioning ingredients help to prevent skin from becoming dry, even with frequent use. Gentle enough to use everywhere, everyday.

Warnings

• For external use only.

• Avoid contact with eyes. Rinse thoroughly with water if this occurs.

• Keep out of the reach of children.

Directions

• Apply to wet skin. Gently work into a lather and rinse well. Follow with the Nu Skin® body moisturizer of your choice.

Inactive Ingredients

Water (Aqua), Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Aloe Barbadensis Leaf Juice, PPG-2 Hydroxyethyl Coco/Isostearamide, Citrus Paradisi (Grapefruit) Fruit Extract, Chamomilla Recutita (Matricaria) Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Lavandula Angustifolia (Lavender) Extract, Echinacea Angustifolia Extract, PEG-150 Distearate, PEG/PPG-18/18 Dimethicone, Butylene Glycol, Cocamidoproply PG-Dimonium Chloride Phosphate, Citric Acid, Disodium EDTA, Fragrance (Parfum), Methylchloroisothiazolinone, Methylisothiazolinone, Chlorophyllin-Copper Complex (CI 75810).

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 500 ml Bottle Label

NU SKIN

antibacterial
body cleansing gel

500 ml e (16.9 fl. oz.)

INGREDIENTS AND APPEARANCE

NU SKIN   ANTIBACTERIAL BODY CLEANSING
triclosan gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-0271
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	0.55 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Grapefruit (UNII: O82C39RR8C)
Matricaria Recutita (UNII: G0R4UBI2ZZ)
Rosemary Oil (UNII: 8LGU7VM393)
Lavandula Angustifolia Flowering Top (UNII: 9YT4B71U8P)
Echinacea Angustifolia (UNII: VB06AV5US8)
PEG-150 Distearate (UNII: 6F36Q0I0AC)
Butylene Glycol (UNII: 3XUS85K0RA)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Edetate Disodium (UNII: 7FLD91C86K)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Methylisothiazolinone (UNII: 229D0E1QFA)
Sodium Copper Chlorophyllin (UNII: 1D276TYV9O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-0271-8	250 mL in 1 BOTTLE, PLASTIC
2	NDC: 62839-0271-9	500 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	08/26/1996

Labeler - NSE Products, Inc. (966817975)