OTC Medication Information: Workforce Foaming Hand Sanitizer E3

WORKFORCE FOAMING HAND SANITIZER E3- benzalkonium chloride liquid
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

ACTIVE INGREDIENT

Benzalkonium Chloride ………..0.1%

Purpose

Antimicrobial

Uses

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use.

Warnings For external use only.

When Using this Product

  • Avoid contact with eyes. In case of eye contact, flush eyes with water. Do not ingest.
  • Stop use and ask a doctor if irritation or redness develops and conditions persist.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

-Pump a small amount of foam into palm of hand.

-Rub thoroughly over all surfaces of both hands.

-Rub hands together brisky until dry

Inactive Ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, Citric Acid.

Workforce Foaming Hand Sanitizer E3

Safely formulated to kill dangerous microorganiss. Pre-lathered for quick, convenient dispensing, which leaves little room for mess. Dye & Fragrance free.

1 gallon

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2 x 1

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4×1

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WORKFORCE FOAMING HAND SANITIZER E3
foaming hand sanitizer e3 liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:50241-430
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.1 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER
CETRIMONIUM CHLORIDE
LAURTRIMONIUM CHLORIDE
DIHYDROXYETHYL COCAMINE OXIDE
GLYCERETH-17 COCOATE
CITRIC ACID MONOHYDRATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50241-430-01 3785 g in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 05/29/2020
Labeler — Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. (028311595)
Registrant — Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. (028311595)
Establishment
Name Address ID/FEI Operations
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. 028311595 manufacture (50241-430), api manufacture (50241-430), pack (50241-430)

Revised: 05/2020 Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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