VIDA MIA MERTHIOLATE- benzalkonium chloride liquid
Nvarro Discount Pharmacies, LLC

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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Vida Mia Merthiolate

DDM Merthiolate

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Indications

First aid antiseptic to help skin infection in minor: cuts, scrapes, burns, insect bites.

Warnings

For external use only.

Ask a doctor before use if you have

Deep or puncture wounds

Animal bites

Serious burns

When using this product do not

Get into the eyes

Apply over large areas of the body

Apply over raw surfaces or blistered areas

Use longer than one week unless directed by doctor.

Stop use and ask a doctor if

Redness, swelling or pain persists or increases.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately. Soap will deactivate the effects of this product.

Directions

Adults and children 2 years and older. Clean the affected area; apply a small amount on the area 1 to 3 times daily; may be covered with a sterile bandage. If bandaged, let dry first.
Children under 2 yrs. of age: Consult a doctor.

Inactive Ingredient

Acetone, FD&C Red No 4. Purified water.

Label

VIDA MIA MERTHIOLATE
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:59970-749
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)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:59970-749-92	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/09/2017	03/31/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	11/09/2017	03/31/2018

Labeler - Nvarro Discount Pharmacies, LLC (094930963)

Registrant - Humco Holding Group, Inc. (825672884)

Name	Address	ID/FEI	Business Operations
Establishment
Humco Holding Group, Inc.		825672884	manufacture(59970-749) , analysis(59970-749) , pack(59970-749) , label(59970-749)

Revised: 11/2018

Document Id: 7a3f0b38-0210-ead8-e053-2991aa0aaaf6

Set id: 5d9055dd-91be-30fd-e053-2a91aa0a8071

Version: 2

Effective Time: 20181109

Nvarro Discount Pharmacies, LLC