OTC Medication Information: Workforce Foaming Hand Sanitizer E3

WORKFORCE FOAMING HAND SANITIZER E3- benzalkonium chloride soap
Magnus Procurement & Logistics Solution, Inc.

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.

Active Ingredient Purpose

Benazlkonium Chloride 0.1%……………….Antimicrobial

Uses

For hand sanitizing to decrease bacteria on the skin.

Recommended for repeated use.

When using this product Avoid contact with eyes. In case of eye contact, flush eyes with water. Do not ingest.

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 surffaces of both hands

Rub hands together briskly until dry.

Inactive Ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide

Stop use and ask a doctor if irritation or redness develops and conditions persist.

Antiseptic, Hand Sanitizer

Warnings For External use only.

1 gl label
(click image for full-size original)

1.25 L Front Label
(click image for full-size original)

1.25 L Back Label
(click image for full-size original)

WORKFORCE FOAMING HAND SANITIZER E3
benzalkonium chloride soap
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:81122-120
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 0.1 g
Inactive Ingredients
Ingredient Name Strength
WATER
CETRIMONIUM CHLORIDE
LAURTRIMONIUM CHLORIDE
DIHYDROXYETHYL COCAMINE OXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:81122-120-01 3785 g in 1 BOTTLE, PLASTIC None
2 NDC:81122-120-50 1250 g in 1 CARTRIDGE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 11/18/2020
Labeler — Magnus Procurement & Logistics Solution, Inc. (012763630)
Registrant — Seatex, LLC (026647404)
Establishment
Name Address ID/FEI Operations
Seatex, LLC 026647404 label (81122-120), manufacture (81122-120), pack (81122-120)

Revised: 11/2020 Magnus Procurement & Logistics Solution, 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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