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

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

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

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

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

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M003	03/22/2013

Labeler - DLC Laboratories, Inc (093351930)

Registrant - Pharma Nobis, LLC (118564114)

Name	Address	ID/FEI	Business Operations
Establishment
Pharma Nobis, LLC		118564114	analysis(24286-1532) , manufacture(24286-1532) , pack(24286-1532) , label(24286-1532)

De La Cruz Tincture Merthiolate