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  4. NDC Product Code: 11509-5282 Omv Anti-itch Bikini

NDC 11509-5282 Omv Anti-itch Bikini

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11509-5282?
  4. Omv Anti-itch Bikini 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:
11509-5282
Proprietary Name:
Omv Anti-itch Bikini
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Combe Incorporated
Labeler Code:
11509
Product Label ID:
284064af-299d-4517-9cef-191382e264d7
Start Marketing Date: [9]
01-01-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 11509-5282?

The NDC code 11509-5282 is assigned by the FDA to the product Omv Anti-itch Bikini which is product labeled by Combe Incorporated. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11509-5282-1 1 tube in 1 carton / 48 g in 1 tube. 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 Omv Anti-itch Bikini?

Apply to irritated and chafed skin as often as needed for instant relief.

Which are Omv Anti-itch Bikini UNII Codes?

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

Which are Omv Anti-itch Bikini 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".