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Signatry Antibacterial Plum Foam Handwash

Medically reviewed on June 14, 2017

Dosage form: liquid
Ingredients: Benzalkonium Chloride 0.005mg in 1mL
Labeler: GOJO Industries, Inc.
NDC Code: 21749-545

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.

Signatry Antibacterial Plum Foam Handwash

Active ingredient

Benzalkonium Chloride 0.5%

Purpose

Antimicrobial

Uses

• Handwash to help decrease bacteria on the skin

• Recommended for repeated use

Warnings

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts

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

Directions

• Wet hands

• Apply a small amount of product and work into a lather

• Rinse well and dry hands completely

Inactive Ingredients

Water (Aqua), Propylene Glycol, Glycerin, Cocamidopropyl Betaine, PEG-80 Sorbitan Laurate, Citric Acid, Ethylhexylglycerin, Lauramine Oxide, Polyquaternium-10, Fragrance (Parfum), Phenoxyethanol, Blue 1 (CI 42090), Red 33 (CI 17200)

SIGNATRY ANTIBACTERIAL PLUM FOAM HANDWASH 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-545
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (BENZALKONIUM) Benzalkonium Chloride0.005 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Propylene Glycol 
Glycerin 
Cocamidopropyl Betaine 
PEG-80 Sorbitan Laurate 
CITRIC ACID MONOHYDRATE 
Ethylhexylglycerin 
Lauramine Oxide 
POLYQUATERNIUM-10 (10000 MPA.S AT 2%) 
PHENOXYETHANOL 
FD&C BLUE NO. 1 
D&C RED NO. 33 
Packaging
#Item CodePackage Description
1NDC:21749-545-08236 mL in 1 PACKAGE
2NDC:21749-545-97700 mL in 1 PACKAGE
3NDC:21749-545-891200 mL in 1 PACKAGE
4NDC:21749-545-901250 mL in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/14/2017
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534manufacture(21749-545)

 
GOJO Industries, Inc.

Further information

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

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