NDC 70242-130 Mercurochrome
NDC Product Code 70242-130
Proprietary Name: Mercurochrome What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 70242 - Dannso Corp./d.b.a. Essential Products
- 70242-130 - Mercurochrome
NDC 70242-130-01
Package Description: 30 mL in 1 BOTTLE, PLASTIC
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
Dosage Form: -
Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
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 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. Values = ‘Y’ or ‘N’.
* 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
- Otc - Purpose
- Otc - Keep Out Of Reach Of Children
- Indications & Usage
- Dosage & Administration
- Warnings
- Inactive Ingredient
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
- 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.