MERCUROCHROME- benzalkonium chloride solution

Mercurochrome by

Drug Labeling and Warnings

Mercurochrome by is a Otc medication manufactured, distributed, or labeled by Vitamin USA, Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredients: Purpose

Benzalkoinum Chloride 0.13% First Aid Antiseptic

Uses

Uses: First aid to help prevent infection in minor cuts, scrapes, and burns.

Warnings:

Warnings

For External Use Only

Do Not Use: in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor. Longer than 1 week unless directed by doctor.

Stop use and ask a doctor

Stop use and ask a doctor if the condition perssits or gets worse.

If pregannt or breastfeeding

If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

Directions

Clean the affected area. Apply small amount of this product on the area 1 to 3 times daily. Supervise children in the use of this product.

Other Information

Other Information

Store at controlled room temperature: 15-30°C (59-86°F). Tamper Evident Feature: Do not use if cello-band over cap is torn, broken or missing. Close tightly after use.

Inactive ingredients

Inactive ingredients: Purified Water, Alcohol, FD&C #40

Directions

Directions

Clean the affected area. Apply small amount of this product on the area 1 to 3 times daily. Supervise children in the use of this product.

Keep out of reach of children

If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

PRINCIPAL DISPLAY PANEL

Mercuro

Cromo

Mercurochrome

First Aid Antiseptic

For External Use Only

Net Contents: 1 Fl Oz. (30 mL)

INGREDIENTS AND APPEARANCE

MERCUROCHROME 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69469-013
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
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Product Characteristics
Color	red	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69469-013-01	30 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	09/03/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/03/2024

Labeler - Vitamin USA, Corp (054256676)