Label: NU SKIN ANTIBACTERIAL BODY CLEANSING- triclosan gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 62839-0271-8, 62839-0271-9 - Packager: NSE Products, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 13, 2010
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- Uses
- Warnings
- Directions
-
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?
- PRINCIPAL DISPLAY PANEL - 500 ml Bottle Label
-
INGREDIENTS AND APPEARANCE
NU SKIN ANTIBACTERIAL BODY CLEANSING
triclosan gelProduct 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)