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Antibacterial by Sun Products Corporation

Medically reviewed on January 1, 2018

Dosage form: soap
Ingredients: Triclosan .1mL in 100mL
Labeler: Sun Products Corporation
NDC Code: 63691-002

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 Facts

Drug Facts

Active ingredient

Triclosan 0.10% (or % in formula)

Use helps fight germs on hands when used as a hand soap

Warnings

For external use only

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.  In case of eye contact, rinse thoroughly with water.

Purpose

Antibacterial hand soap

Questions? (insert proper phone number)

Directions wash hands and rinse

Inactive ingredients water, .....

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ANTIBACTERIAL 
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-002
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Triclosan (Triclosan) Triclosan.1 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Packaging
#Item CodePackage Description
1NDC:63691-002-01304 mL in 1 BOTTLE
2NDC:63691-002-02384 mL in 1 BOTTLE
3NDC:63691-002-03414 mL in 1 BOTTLE
4NDC:63691-002-04739 mL in 1 BOTTLE
5NDC:63691-002-05828 mL in 1 BOTTLE
6NDC:63691-002-061120 mL in 1 BOTTLE
7NDC:63691-002-071770 mL in 1 BOTTLE
8NDC:63691-002-083785 mL in 1 BOTTLE
9NDC:63691-002-093990 mL in 1 BOTTLE
10NDC:63691-002-10709 mL in 1 BOTTLE
11NDC:63691-002-111005 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/13/1998
Labeler - Sun Products Corporation (070931480)

 
Sun Products Corporation

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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