NDC 68786-411 Vitamins A And D Without Lanolin

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68786-411
Proprietary Name:
Vitamins A And D Without Lanolin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sion Biotext Medical Ltd
Labeler Code:
68786
Start Marketing Date: [9]
01-07-2016
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 68786-411-01

Package Description: 6 BOX in 1 CASE / 144 PACKET in 1 BOX / 5 g in 1 PACKET

Product Details

What is NDC 68786-411?

The NDC code 68786-411 is assigned by the FDA to the product Vitamins A And D Without Lanolin which is product labeled by Sion Biotext Medical Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68786-411-01 6 box in 1 case / 144 packet in 1 box / 5 g in 1 packet. 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 Vitamins A And D Without Lanolin?

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Which are Vitamins A And D Without Lanolin UNII Codes?

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

Which are Vitamins A And D Without Lanolin 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 Vitamins A And D Without Lanolin?

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".