NDC 0924-1805 Acme Small Cuts And Burns

NDC Product Code 0924-1805

NDC 0924-1805-01

Package Description: 1 KIT in 1 KIT * .9 g in 1 PACKAGE (52124-0004-1) * .8 mL in 1 PACKAGE (52124-0001-1) * .5 g in 1 TUBE (52124-0003-1)

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

NDC Product Information

Acme Small Cuts And Burns with NDC 0924-1805 is a product labeled by Acme United Corp.. The generic name of Acme Small Cuts And Burns is . The product's dosage form is and is administered via form.

Labeler Name: Acme United Corp.

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)

Product Labeler Information

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

Labeler Name: Acme United Corp.
Labeler Code: 0924
Start Marketing Date: 04-30-2010 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: 12-31-2018 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: E 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.

Acme Small Cuts And Burns 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:                             Benzalkonium Chloride 0.13%Lidocaine HCL 0.5%

Active Ingredient:                             PurposeBenzalkonium Chloride 0.40%... First Aid Antiseptic

Active Ingredient: .........Bacitracin Zinc 400 unitsNeomycin Sulfate 5mg ( equivalent to 3.5 mg Neomycin base)Polymyxin B Sulfate 5000 units

Otc - Purpose

Purpose: First aid antiseptic, external analgesicUses: First aid to help prevent infection and forthe temporary relief of pain and itching associated with:minor cuts, scrapes, burns

Use: For Professional and Hospital use.  Helpsprevent infection.  Antiseptic cleansing of face,hands and body without soap and water.

Uses:  To help prevent infection in:
minor cuts;  scrapes;  burns

Warnings

Warning:  For external use only.

Warning:    For external use only.

Warnings:For external use only.

Otc - Do Not Use

Do not use:  in eyes, in large quantities, over raw blistered areas, or on deep puncture wounds, animal bites or serious burns, for more than one week

Do not use in the eyes or over large areas of the body.

Do not use:  in eyes;  over large areas of the body; If allergic to any of the ingredients;  for more than one week unless directed by a physician.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.If ingested, contact a Poison Control Center right away.

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

Keep out of reach of children.If ingested, contact a Poison Control Center right away.

Dosage & Administration

Directions: Clean affected area, Apply small amount not more than 3 times daily.May be covered with a sterile bandage.

Storage And Handling

Other Information:Store at room temperature

Other information:Store at room temperature.

Description

LOT/EXP:                                    Made in CHINA20130301

LOT/EXP:                                    Made in CHINA20130301

Otc - Stop Use

Stop use if unusual redness, swelling or other symptoms occur. Consult a physician immediately.

Stop use and consult a doctor:if the condition persists or gets worse;  a rash or other allergic reaction develops

Otc - When Using

Directions: Tear open packet, unfold towelette and use to cleanse desired skin area.  Discardtowelette appropriately after single use.

Directions: clean affected area;  apply small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily; may be covered with a sterile bandage

Inactive Ingredient

Inactive Ingredient:    Purified water

* Please review the disclaimer below.