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  4. NDC Product Code: 81113-101 Pomiks Antiseptic Wet Wipes

NDC 81113-101 Pomiks Antiseptic Wet Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81113-101?
  4. Pomiks Antiseptic Wet Wipes 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:
81113-101
Proprietary Name:
Pomiks Antiseptic Wet Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Boni Kimya Sanayi Ve Ticaret Limited Sirketi
Labeler Code:
81113
Product Label ID:
e0f5917a-2773-441e-942c-438a8dc6dc65
Start Marketing Date: [9]
11-30-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81113-101-10

Package Description: 100 PACKAGE in 1 BOX / 3.3 mL in 1 PACKAGE

NDC Code 81113-101-12

Package Description: 120 PACKAGE in 1 BOX / 3.3 mL in 1 PACKAGE

NDC Code 81113-101-15

Package Description: 15 PACKAGE in 1 BOX / 3.3 mL in 1 PACKAGE

NDC Code 81113-101-20

Package Description: 200 PACKAGE in 1 BOX / 3.3 mL in 1 PACKAGE

NDC Code 81113-101-30

Package Description: 30 PACKAGE in 1 BOX / 3.3 mL in 1 PACKAGE

NDC Code 81113-101-60

Package Description: 60 PACKAGE in 1 BOX / 3.3 mL in 1 PACKAGE

NDC Code 81113-101-72

Package Description: 72 PACKAGE in 1 BOX / 3.3 mL in 1 PACKAGE

NDC Code 81113-101-80

Package Description: 80 PACKAGE in 1 BOX / 3.3 mL in 1 PACKAGE

Product Details

What is NDC 81113-101?

The NDC code 81113-101 is assigned by the FDA to the product Pomiks Antiseptic Wet Wipes which is product labeled by Boni Kimya Sanayi Ve Ticaret Limited Sirketi. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 81113-101-10 100 package in 1 box / 3.3 ml in 1 package, 81113-101-12 120 package in 1 box / 3.3 ml in 1 package, 81113-101-15 15 package in 1 box / 3.3 ml in 1 package, 81113-101-20 200 package in 1 box / 3.3 ml in 1 package, 81113-101-30 30 package in 1 box / 3.3 ml in 1 package, 81113-101-60 60 package in 1 box / 3.3 ml in 1 package, 81113-101-72 72 package in 1 box / 3.3 ml in 1 package, 81113-101-80 80 package in 1 box / 3.3 ml in 1 package. 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 Pomiks Antiseptic Wet Wipes?

Open the cover or seal on the sticker of wet wipeswet hands thoroughly with product and allow to dry without wipingsupervise children under 6 years of age when using this product to avoid swallowingafter use, please close the wet wipes cover or seal the sticker to keep the wet wipes moist.do not dispose in toilet to avoid clogging

Which are Pomiks Antiseptic Wet Wipes UNII Codes?

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

Which are Pomiks Antiseptic Wet Wipes 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 Pomiks Antiseptic Wet Wipes?

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".