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  4. NDC Product Code: 65734-000 3-step First Aid Kit

NDC 65734-000 3-step First Aid Kit

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 65734-000?
  4. 3-step First Aid Kit Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
65734-000
Proprietary Name:
3-step First Aid Kit
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Swabplus Inc.
Labeler Code:
65734
Product Label ID:
4f2dc3fe-9388-4a31-8eff-cfdb2d3501fb
Start Marketing Date: [9]
03-01-2003
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 65734-000?

The NDC code 65734-000 is assigned by the FDA to the product 3-step First Aid Kit which is product labeled by Swabplus Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65734-000-23 1 kit in 1 carton * 2 ml in 1 packet (65734-125-01) * 2 ml in 1 packet (65734-119-01). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for 3-step First Aid Kit?

Do not use if label seal is broken prior to purchase.Hold the swab vertically, with the color ring band tip upwards. Hold in the center of the stem with one hand and at the color band with the other.Bend the tip at the color band to one side until it snaps.Apply the product to the affected area.Discard swab after use.

Which are 3-step First Aid Kit UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are 3-step First Aid Kit Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for 3-step First Aid Kit?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".