NDC 0159-2200 Selan Plus Zinc Oxide

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:
0159-2200
Proprietary Name:
Selan Plus Zinc Oxide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
0159
Start Marketing Date: [9]
08-29-1997
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 0159-2200?

The NDC code 0159-2200 is assigned by the FDA to the product Selan Plus Zinc Oxide which is product labeled by Trividia Manufacturing Solutions, Inc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 0159-2200-01 8.1 g in 1 packet , 0159-2200-04 117 g in 1 tube , 0159-2200-17 458 g in 1 jar . 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 Selan Plus Zinc Oxide?

Apply cream liberally as often as necessarychange wet and soiled diapers promptlycleanse the diaper area, and allow to dryapply cream with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged

Which are Selan Plus Zinc Oxide UNII Codes?

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

Which are Selan Plus Zinc Oxide 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 Selan Plus Zinc Oxide?

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".