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Joy Non-ultra

Dosage form: soap
Ingredients: Triclosan 0.1g in 100mL
Labeler: Procter & Gamble Manufacturing Company
NDC Code: 37000-609

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.

Joy Non-Ultra Orange AB

DRUG FACTS

Active Ingredient

Triclosan 0.10%

Purpose

Antibacterial hand soap

Use
  • For handwashing to decrease bacteria on the skin

Warnings

For external use only

Keep out of reach of children.

In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

Directions
  • Wet hands and forearms. Apply 5 ml or palmful to hands and forearms. Scrub thoroughly for 90 sec. Rinse and repeat.

Inactive ingredients

water, sodium lauryl sulfate, sodium laureth sulfate, lauramine oxide, sodium chloride, phenoxyethanol, PEI-14 PEG-10/PPG-7 copolymer, methylisothiazolinone, fragrance, yellow 5, red 33.

Questions?

1-800-436-1569

Distributed by PROCTER & GAMBLE, CINCINNATI, OH 45202.

PRINCIPAL DISPLAY PANEL - 414 mL Bottle Label

Great
Cleaning!
Great Price!

non-ultra
ⓊJoy®
Antibacterial
hand soap

dishwashing liquid

FPO

orange
scent

414 mL
14 FL OZ

99713191

JOY NON-ULTRA 
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-609
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Triclosan (Triclosan) Triclosan0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURYL SULFATE 
SODIUM LAURETH SULFATE 
LAURAMINE OXIDE 
SODIUM CHLORIDE 
PHENOXYETHANOL 
METHYLISOTHIAZOLINONE 
FD&C YELLOW NO. 5 
D&C RED NO. 33 
Product Characteristics
ColorORANGEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:37000-609-14414 mL in 1 BOTTLE, PLASTIC
2NDC:37000-609-15443 mL in 1 BOTTLE, PLASTIC
3NDC:37000-609-16473 mL in 1 BOTTLE, PLASTIC
4NDC:37000-609-561660 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E02/01/2011
Labeler - Procter & Gamble Manufacturing Company (004238200)
Establishment
NameAddressID/FEIOperations
The Procter & Gamble Manufacturing Company007130032ANALYSIS, LABEL, MANUFACTURE, PACK, RELABEL, REPACK

Revised: 10/2011
Document Id: bcf33ea8-38b6-41fb-9fb6-2f442b1fb79f
Set id: ba5aee12-1c60-4752-8375-946157aa7b8a
Version: 2
Effective Time: 20111025
 
Procter & Gamble Manufacturing Company

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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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