NDC 70242-130 Mercurochrome

NDC Product Code 70242-130

NDC 70242-130-01

Package Description: 30 mL in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Mercurochrome with NDC 70242-130 is a product labeled by Dannso Corp./d.b.a. Essential Products. The generic name of Mercurochrome is . The product's dosage form is and is administered via form.

Labeler Name: Dannso Corp./d.b.a. Essential Products

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Dannso Corp./d.b.a. Essential Products
Labeler Code: 70242
Start Marketing Date: 01-01-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Mercurochrome Product Label Images

Mercurochrome Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active Ingredients                                                   PurposeBenzalkonium Chloride (0.13%) ................... First aid antiseptic

Otc - Purpose

  • UseMay help prevent skin infection inminor cutsscrapes burns

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Indications & Usage

MercurochromeMercury FreeFirst Aid AntisepticFor External Use Only

Dosage & Administration

  • Directionsclean the affected areaand dry thoroughly. Apply a thin layer 1 to 3 times daily.May be covered with a sterile bandage, let dry first.


  • Warnings For external use onlyAvoid Contact with eyes.When using this productdo not use on irritated skin, in or near eyes or mocous membranes, on wounds or damaged skin, if prone to allergic reactionFatal if swallowed.Stop use and ask a doctor if condition persists or gets worse

Inactive Ingredient

Inactive Ingredients purified water, Isopropyl Alcohol, FD&C red # 40.

* Please review the disclaimer below.