ABLS Original Scent

Dosage form: liquid
Ingredients: TRICLOSAN 0.7458g in 237mL
Labeler: Melaleuca, Inc.
NDC Code: 54473-109

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.

ABLS Original 8 oz Content of Label

Active Ingredient
Triclosan 0.3%

Purpose
Antibacterial

Use
for handwashing to decrease bacteria on the skin

Warnings
For external use only

When using this product

  • avoid contact with eyes. In case of eye contact, flush with water.
  • discontinue use if signs of irritation or rash appear. If irritation or rash persists for more than three days, consult a physician.

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

Inactive ingredients
butylene glycol, citric acid, cocamidopropyl betaine, disodium oleamido MIPA sulfosuccinate, glycerin, glycol distearate, helianthus annuus (sunflower) seed oil, melaleuca alternifolia (tea tree) leaf oil (T36-C5® brand), phenoxyethanol, polyquaternium 10, potassium sorbate, prunus armeniaca (apricot) kernel oil, simmondsia chinensis (jojoba) seed oil, sodium chloride, sodium coco-sulfate, tocopheryl acetate (vitamin E acetate), water

Directions

  • pump into hands
  • lather vigorously for at least 15 seconds
  • rinse and dry thoroughly
ABLS  ORIGINAL SCENT
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54473-109
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN0.7458 g  in 237 mL
Inactive Ingredients
Ingredient NameStrength
BUTYLENE GLYCOL 
ANHYDROUS CITRIC ACID 
COCAMIDOPROPYL BETAINE 
Glycerin 
GLYCOL DISTEARATE 
SUNFLOWER OIL 
Tea Tree Oil 
PHENOXYETHANOL 
POLYQUATERNIUM-10 (400 CPS AT 2%) 
POTASSIUM SORBATE 
APRICOT SEED OIL 
JOJOBA OIL 
SODIUM CHLORIDE 
SODIUM COCO-SULFATE 
ALPHA-TOCOPHEROL ACETATE 
Water 
Packaging
#Item CodePackage Description
1NDC:54473-109-08237 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/01/2006
Labeler - Melaleuca, Inc. (139760102)
Establishment
NameAddressID/FEIOperations
Melaleuca, Inc.139760102manufacture

Revised: 01/2011
 
Melaleuca, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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