NDC 81459-302 Repuera Dermatozyme 5% Ultra Moisture Cream

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:
81459-302
Proprietary Name:
Repuera Dermatozyme 5% Ultra Moisture Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
81459
Start Marketing Date: [9]
01-28-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 81459-302?

The NDC code 81459-302 is assigned by the FDA to the product Repuera Dermatozyme 5% Ultra Moisture Cream which is product labeled by Alluv. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81459-302-01 80 ml 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 Repuera Dermatozyme 5% Ultra Moisture Cream?

Apply the cream to affected area and massage gently into the skin.

Which are Repuera Dermatozyme 5% Ultra Moisture Cream UNII Codes?

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

Which are Repuera Dermatozyme 5% Ultra Moisture Cream 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".