DE LA CRUZ MERCUROCHROME - benzalkonium chloride and lidocaine hydrochloride liquid
DLC Laboratories, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Mercurochrome

Active Ingredients

Benzalkonium Chloride 0.13%

Liddocaine Hydrochloride 2.5%

Purpose

First Aid Antiseptic

Pain Reliever

Uses

first aid to help prevent bacterial contamination or skin infection and temporarily relieves pain and itching associated with cuts, scrapes, burns, sunburn, skin irritations

Warnings

For external use only.

Ask a dotor 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 ares of the body or in large quantities. do not apply over raw surfaces or blistered areas.

Stop use and ask a doctor if

condition worsens, symptoms persist for more than 7 days, or clear up and occur again with in a few days.

Keep out of the reach of children

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

Directions

adults and children 2 years of age and older: 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 (let dry first). children unde4r 2 years, ask a doctor

Other Information

protect from excessive heat

Inactive Ingredients

acetone, purified water USP

De La Cruz

Mercurochrome

(Benzalkonium Chloride and Lidocaine hydrochloride)

Helps prevent skin infection and relieves pain and itching in minor cuts, scrapes, burns and insect bites.
FIRST AID ANTISEPTIC AND PAIN RELIEVER

Mercury Free
Contents 1fl oz (30mL)

Manufactured by
DLC Laboratories, Inc.
PARAMOUNT, CA 90723 USA

1-800-858-3889 / www.dlclabs.com

Mercurochrome

DE LA CRUZ MERCUROCHROME
benzalkonium chloride and lidocaine hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:24286-1553
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g in 100 mL
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	2.5 g in 100 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:24286-1553-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/30/2011	08/31/2015

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	06/30/2011	08/31/2015

Labeler - DLC Laboratories, Inc. (093351930)

Registrant - DLC Laboratories, Inc. (093351930)

Name	Address	ID/FEI	Business Operations
Establishment
DLC Laboratories, Inc.		093351930	manufacture(24286-1553)

Revised: 6/2017

Document Id: 1abb785e-b7bc-49b1-b94b-c8da1eeb9779

Set id: f9587a3e-179a-4b39-806d-627f6372074f

Version: 2

Effective Time: 20170607

DLC Laboratories, Inc.