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  4. NDC Product Code: 61924-504 Lantiseptic By Dermarite Dry Skin Therapy

NDC 61924-504 Lantiseptic By Dermarite Dry Skin Therapy

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 61924-504?
  4. Lantiseptic By Dermarite Dry Skin Therapy 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:
61924-504
Proprietary Name:
Lantiseptic By Dermarite Dry Skin Therapy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dermarite Industries Llc
Labeler Code:
61924
Product Label ID:
7730af3b-fea2-63ee-e053-2991aa0afe0c
Start Marketing Date: [9]
12-25-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61924-504-04

Package Description: 113 g in 1 TUBE

NDC Code 61924-504-05

Package Description: 5 g in 1 PACKET

NDC Code 61924-504-14

Package Description: 14.2 g in 1 PACKET

Product Details

What is NDC 61924-504?

The NDC code 61924-504 is assigned by the FDA to the product Lantiseptic By Dermarite Dry Skin Therapy which is product labeled by Dermarite Industries Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 61924-504-04 113 g in 1 tube , 61924-504-05 5 g in 1 packet , 61924-504-14 14.2 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 Lantiseptic By Dermarite Dry Skin Therapy?

Apply liberally to affected area as needed or as directed by a physician.

Which are Lantiseptic By Dermarite Dry Skin Therapy UNII Codes?

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

Which are Lantiseptic By Dermarite Dry Skin Therapy 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 Lantiseptic By Dermarite Dry Skin Therapy?

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".