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.

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De La Cruz Tincture Merthiolate

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

First Aid Antiseptic

Uses

First aid antiseptic to help prevent infection in minor:

cuts - scrapes - burns

Warnings

For external use only.

Flammable. Keep away from sparks, heat and fire.

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
  • do not use longer than 1 week unless directed by a doctor

Stop use and consult a doctor if

  • the condition persists or gets worse

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 Merthiolate

Tincture Merthiolate

48% Alcohol

Mercury Free

First Aid Antiseptic

For External Use Only

1 FL OZ (30 mL)

Distributed by

De La Cruz Products

A Division of DLC Laboratories, Inc.

Paramount, CA 90723 USA

Questions: 1-800-858-3889

www.dlclabs.com

Warnings: FLAMMABLE, KEEP AWAY FROM SPARKS, HEAT AND FIRE.

TINCTURE MERTHIOLATE 
benzalkonium chloride tincture
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1532
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ACETONE (UNII: 1364PS73AF)  
ALCOHOL (UNII: 3K9958V90M)  
D&C RED NO. 22 (UNII: 1678RKX8RT)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1532-730 mL in 1 BOTTLE; Type 0: Not a Combination Product12/13/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/22/2013
Labeler - DLC Laboratories, Inc (093351930)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114analysis(24286-1532) , manufacture(24286-1532) , pack(24286-1532) , label(24286-1532)

Revised: 3/2022
Document Id: da6c0721-dfb7-0192-e053-2a95a90a1ac3
Set id: 4fec9119-fbbf-4fc7-9122-c6300cac8731
Version: 7
Effective Time: 20220317
 
DLC Laboratories, Inc