EL VALLE MERTHIOLATE- benzalkonium chloride liquid

El Valle Merthiolate by

Drug Labeling and Warnings

El Valle Merthiolate by is a Otc medication manufactured, distributed, or labeled by Pharmadel LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Drug facts

Active Ingredient & Purpose

• Active ingredient: Purpose
• Benzalkonium chloride 0.13%.............:

  First aid antiseptic

Uses

First aid to help prevent infection in

• minor cuts
• scrapes
• burns

Warnings

FOR EXTERNAL USE ONLY.

Do not use

• longer than 1 week, unless directed by a doctor
• in the eyes
• over large areas of the body

Ask a doctor before use if you have

• a deep or puncture wounds
• serious burns
• animal bites

Stop use and consult a doctor if

• conditions persist or gets worse

Keep out of reach of children.

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

Directions

• clean the affected area
• apply a small amount directly to the affected area 1 to 3 times a day
• may cover area with a sterile bandage

Other information

• do not use if clear seal over cap is missing or broken

Inactive ingredients

alcohol, FD&C red #40, water

Prinicpal Display Panel

INGREDIENTS AND APPEARANCE

EL VALLE MERTHIOLATE 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55758-375
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
FD&C RED NO. 40 (UNII: WZB9127XOA)
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55758-375-01	15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/31/2023	05/31/2023
2	NDC: 55758-375-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	05/31/2023

Labeler - Pharmadel LLC (030129680)