TINCTURE MERTHIOLATE- benzalkonium chloride tincture 
DLC Laboratories, 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.

----------

Tincture Merthiolate

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

First Aid Antiseptic

Uses

first aid to help prevent infection in minor:
cuts - scrapes - burns - insect bites

Warnings

For external use only.
Consult a doctor before use if you have - deep or puncture wounds - animal bites - serious burns

When using this product

  • do not use in or near the eyes
  • do not apply in large quantities or over large areas of the body
  • do not apply over raw surtaces or blistered areas

Stop use and consult a doctor if

  • redness, irritation, swelling or pain persists or increases, or il infection or rash occurs
  • symptoms persist for more than 7 days, or clear up and occur again within a lew days

Keep out of reach of children.

II swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Other Information

Inactive Ingredients

acetone, alcohol, DandC red no. 22, purified water

Product Labeling

De La Cruz

Tincture Merthiolate

50% Alcohol

Mercury Free

For external use only

First Aid Antiseptic

1 FL OZ

Manufactured by
De La Cruz Products
A Division of DLC Laboratories, Inc.
Paramount, CA 90723 USA
Questions: 1-800-858-3889
www.dlclabs.com

Warnings: do not use if plastic seal around cap is broken or removed. For external use only.

Merthiolate Tincture

TINCTURE MERTHIOLATE 
benzalkonium chloride tincture
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:24286-1532
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ACETONE 
ALCOHOL 
D&C RED NO. 22 
WATER 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1532-730 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/22/2013
Labeler - DLC Laboratories, Inc (093351930)

Revised: 3/2013
Document Id: 8c9ecb50-d598-4055-93f7-64a9f5b0b54a
Set id: 4fec9119-fbbf-4fc7-9122-c6300cac8731
Version: 1
Effective Time: 20130322
 
DLC Laboratories, Inc