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  4. NDC Product Code: 77283-002 Onko Health Alcohol Antiseptic Wipe

NDC 77283-002 Onko Health Alcohol Antiseptic Wipe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 77283-002?
  4. Onko Health Alcohol Antiseptic Wipe Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
77283-002
Proprietary Name:
Onko Health Alcohol Antiseptic Wipe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Onko Pharmaceuticals Usa Inc.
Labeler Code:
77283
Product Label ID:
a7af4ea8-a84a-4431-92f7-181fabed98d6
Start Marketing Date: [9]
07-13-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 77283-002?

The NDC code 77283-002 is assigned by the FDA to the product Onko Health Alcohol Antiseptic Wipe which is product labeled by Onko Pharmaceuticals Usa Inc.. The product's dosage form is . The product is distributed in 16 packages with assigned NDC codes 77283-002-01 1 not applicable in 1 pouch / 5 ml in 1 not applicable, 77283-002-02 100 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-03 120 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-04 150 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-05 350 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-06 400 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-07 450 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-08 500 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-09 550 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-10 600 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-11 700 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-12 800 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-13 900 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-14 1000 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-15 2000 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable, 77283-002-16 5000 not applicable in 1 bottle, plastic / 3.12 ml in 1 not applicable. 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 Onko Health Alcohol Antiseptic Wipe?

For single pack;• Tear open pouch, remove towel.• Wipe injection site vigorously and discard. / Wet hands and wrists thoroughly for 15 seconds and discard.• Supervise children under 6 years of age.For multi pack;• Open clip-lid.• Remove moist towels to clean skin as required.• Wipe injection site vigorously and discard. / Wet hands and wrists thoroughly for 15 seconds and discard.• Close lid when not in use to keep remaining towels moist.• Supervise children under 6 years of age.

Which are Onko Health Alcohol Antiseptic Wipe UNII Codes?

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

Which are Onko Health Alcohol Antiseptic Wipe 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:

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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".