Lite nFoamy E3 Hand Sanitizer description, usages, side effects, indications, overdosage, supplying and lots more!

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Lite nFoamy E3 Hand Sanitizer

Spartan Chemical Company


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredients

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.

Stop use and ask a doctor if irritation and redness develops, or if condition persists for more than 72 hours.

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

Directions

  • Hands must be washed and rinsed with potable water before use.
  • Pump a small amount of foam into palm of hand.
  • Rub thoroughly over all surfaces of both hands.
  • Rub hands together briskly until dry.

Other Information

  • This product must be dispensed from an adequate dispenser located a sufficient distance from processing line to prevent accidental product contamination.
  • Do not contaminate water, food or feed by storage and disposal.

Inactive Ingredients

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

Questions?

1 -800-537-8990

Principal Display Panel - Container Label

Spartan ®

Lite'nFoamy ®

E3 Hand Sanitizer

Foam Hand Sanitizer- Fragrance Free

  • Quickly works to reduce the bacteria on the hands in 15 seconds
  • Recommended for use by food service and food processing personnel

FOR INSTITUTIONAL AND INDUSTRIAL USE ONLY

See back panel for additional information.

Manufactured by
Spartan Chemical Company, Inc.

1110 Spartan Drive, Maumee, OH 43537 USA

Medical Emergency: 888-314-6171 / www.spartanchemical.com

Net Contents: 1 U.S. Gallon / 3.79 Liters

Lite nFoamy E3 Hand Sanitizer

Benzalkonium Chloride SOAP

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64009-334
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 1.0 g

Inactive Ingredients

Ingredient Name Strength
water
CETRIMONIUM CHLORIDE
LAURTRIMONIUM CHLORIDE
GLYCERETH-17 COCOATE
dihydroxyethyl cocamine oxide
CITRIC ACID MONOHYDRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64009-334-05 3.79 in 1 CONTAINER
2 NDC:64009-334-08 280.20 in 1 CONTAINER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2014-04-01


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