WHITE MERTODOL- benzalkonium chloride liquid

White Mertodol by

Drug Labeling and Warnings

White Mertodol by is a Otc medication manufactured, distributed, or labeled by Laboratorios Jaloma, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

First aid to help prevent infection in *minor cuts *scrapes *burns

WARNINGS

Warnings
For external use only

DO NOT USE

Do not use in the eyes or apply over large areas of
the body
Do not use longer than 1 week, unless directed by a
doctor

ASK DOCTOR

Consult a doctor in case of * deep puncture
wounds * animal bites * serious burns

STOP USE

Stop use and consult a doctor if the condition

persists or gets worse

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.  In case of

accidental ingestion, seek professional assistance

or contact a Poison Control Center immediately.

Directions

Clean the affected area *apply a small amount of this product on the area 1 to 3 times daily * may be covered with a sterile bandage

Inactive Ingredients

acetone, alcohol, water

QUESTIONS

Questions

(33) 3617 5010 (In Guadalajara, Jal. Mexico)

White Mertodol

INGREDIENTS AND APPEARANCE

WHITE MERTODOL  
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65055-301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ACETONE (UNII: 1364PS73AF)
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65055-301-01	25 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/24/2016
2	NDC: 65055-301-02	40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/24/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/25/2013

Labeler - Laboratorios Jaloma, S.A. de C.V. (811122357)

Establishment
Name	Address	ID/FEI	Business Operations
Laboratorios Jaloma, S.A. de C.V.		811122357	manufacture(65055-301)