Label: ANTIBACTERIAL BODY WASH MOISTURIZING- triclosan soap

  • 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 September 22, 2010

If you are a consumer or patient please visit this version.

View All Sections
  • Active Ingredient

    Triclosan 0.15%

  • Purpose

    Antibacterial

  • Warnings

    For external use only.

    When using this product

    - Avoid contact with eyes. If contact occurs, rinse with water.

    Stop using this product and ask doctor if

    - Irritation and redness develop.

    Keep out of reach of children.

    In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

  • Questions?

    Call: 1-800-910-6874

  • Use

    For washing to decrease bacteria on skin.

  • Directions

    - squeeze onto wet hands or body sponge

    - work into a lather

    - wash skin, rinse, and dry thoroughly

  • Inactive Ingredients

    Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, PEG-8, Fragrance (Parfum), Glycerin, Isostearoamidopropyl Morpholine Lactate, Polyquaternium-10, Cocamidopropyl PG-Dimonium Chloride, DMDM Hydantoin, Citric Acid, Tetrasodium EDTA, Sodium Chloride, Blue 1 (Cl 42090), Red 33 (Cl 17200).

  • PACKAGE FRONT AND BACK LABELS

    24OZ FRONT AND BACK LABELS: upup24.jpg24OZ Front and Back Lables

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL BODY WASH  MOISTURIZING
    triclosan soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-801
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.15 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-801-24709.7 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/22/2010
    Labeler - Target Corporation (006961700)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!