NDC 44224-0299 Easy Care First Aid

NDC Product Code 44224-0299

NDC 44224-0299-3

Package Description: 1 KIT in 1 KIT * .8 mL in 1 PACKAGE (52124-0001-1) * .5 mL in 1 PACKAGE (52124-0008-1) * .5 g in 1 TUBE (52124-0003-1)

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

NDC Product Information

Easy Care First Aid with NDC 44224-0299 is a product labeled by Tender Corp Dba Adventure Medical Kits. The generic name of Easy Care First Aid is . The product's dosage form is and is administered via form.

Labeler Name: Tender Corp Dba Adventure Medical Kits

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)
  • WATER (UNII: 059QF0KO0R)
  • 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: Tender Corp Dba Adventure Medical Kits
Labeler Code: 44224
Start Marketing Date: 04-07-2011 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.

Easy Care First Aid 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

DRUG FACTS:    Active Ingredient                           purposeBenzalkonium Chloride 0.40%         First Aid Antiseptic

DRUG FACTS- Insect Sting Relief PadActive Ingredient:                  PurposeBenzocaine, 6% w/v            topical anestheticSD Alcohol, 60% w/v         Antiseptic

Otc - Purpose

PurposeFirst Aid Antiseptic

Indications & Usage

For professional and hospital use. helps prevent infection. antiseptic cleansing of face hand and body without soap and water.

Use: For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

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


Warnings: For external use only.

Warnings: For external use only. Keep out of reach of children. If Swallowed get medical help or contact a Poison Control Center right away.  Flammable - keep away from fire or flame. Avoid contact with eyes. If this happens, rinse thoroughly with water.

For external use only.

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. If unusual redness, swelling or other symptoms occur, consult a physician immediately.

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

Otc - Do Not Use

Do Not Use: In the eyes, or over large areas of the body

Do not use: in eyes on broken skin, deep puncture wounds. If unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately

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.

Dosage & Administration

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

Inactive Ingredient

Inactive Ingredient: Purified Water


Active Ingredients

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


Triple Antibiotic

Otc - Stop Use

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


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

Storage And Handling

Other information:Store at room temperature.

* Please review the disclaimer below.