TINCTURE MERTHIOLATE- benzalkonium chloride tincture

Tincture Merthiolate by

Drug Labeling and Warnings

Tincture Merthiolate by is a Otc medication manufactured, distributed, or labeled by DLC Laboratories, Inc, Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

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 over large areas of the body
• do not apply over raw surfaces 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.

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

Directions

• adults and children 2 years of age and older:
  • clean the affected area
  • apply a small amount of this product to the area 1 to 3 times daily
  • may be covered with a sterile bandage. If bandaged, let dry first.
• children under 2 years of age: ask a doctor

Other information

• will stain skin and clothing

Inactive ingredients

acetone, alcohol, D&C red no. 22, purified water

Questions

1-800-858-3889

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Distributed by:
De La Cruz Products
A Division of DLC Laboratories, Inc.
Paramount, CA 90723 USA

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Label

De La Cruz®

Tincture
Merthiolate

48%
Alcohol

Mercury-Free

First Aid Antiseptic

TRUSTED
QUALITY

For External Use Only

1 FL OZ
(30 mL)

INGREDIENTS AND APPEARANCE

TINCTURE MERTHIOLATE 
benzalkonium chloride tincture

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24286-1532
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ACETONE (UNII: 1364PS73AF)
ALCOHOL (UNII: 3K9958V90M)
D&C RED NO. 22 (UNII: 1678RKX8RT)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24286-1532-7	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/13/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/22/2013

Labeler - DLC Laboratories, Inc (093351930)

Registrant - Humco Holding group, Inc. (825672884)