Derma-San: Package Insert and Label Information

DERMA-SAN- benzalkonium chloride liquid
Anderson Chemical Company

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.

Benzalkonium Chlorine, 0.1% w/v

Purpose

Antimicrobial

Use

  • For handwashing to decrease bacteria on skin
  • Recommended for repeated use

Warning

For external use only

When using this product

  • avoid contact with eyes.
  • in case on eye contact, flush eyes with water

Stop use and ask a doctor if

  • irritation or 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

  • Pump a small amounts of foam into palm of hand.
  • Rub thoroughly over all surfaces of both hands.
  • Rub hands together briskly until dry.

Inactive ingredients

Water, cetrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, and citric acid.

Questions or comment?

320-693-2477

Principal Display Panel

Derma-San

NO-RINSE HAND SANITIZER

NET CONTENTS: 1 US GALLON

ProductLabel
(click image for full-size original)
DERMA-SAN
benzalkonium chloride liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:63131-0006
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 1 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
CETRIMONIUM CHLORIDE
DIHYDROXYETHYL COCAMINE OXIDE
LAURTRIMONIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63131-0006-1 7570 JUG in 1 CASE contains a JUG
1 3785 mL in 1 JUG This package is contained within the CASE (63131-0006-1)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 05/20/2008
Labeler — Anderson Chemical Company (006179220)
Establishment
Name Address ID/FEI Operations
Anderson Chemical Company 006179220 manufacture (63131-0006)

Revised: 05/2020 Anderson Chemical Company

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