NDC 51393-4007 Scabies Control

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:
51393-4007
Proprietary Name:
Scabies Control
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Forces Of Nature
Labeler Code:
51393
Start Marketing Date: [9]
03-15-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)

Product Packages

NDC Code 51393-4007-1

Package Description: 1 BOTTLE, DISPENSING in 1 BOX / 11 mL in 1 BOTTLE, DISPENSING

NDC Code 51393-4007-2

Package Description: 1 BOTTLE, DISPENSING in 1 BOX / 33 mL in 1 BOTTLE, DISPENSING

Product Details

What is NDC 51393-4007?

The NDC code 51393-4007 is assigned by the FDA to the product Scabies Control which is product labeled by Forces Of Nature. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 51393-4007-1 1 bottle, dispensing in 1 box / 11 ml in 1 bottle, dispensing, 51393-4007-2 1 bottle, dispensing in 1 box / 33 ml in 1 bottle, dispensing. 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 Scabies Control?

Use to treat scabies symptoms, skin rash, itch and irritation. Use after diagnosis by a physician.

Which are Scabies Control UNII Codes?

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

  • THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)
  • THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (Active Moiety)

Which are Scabies Control 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:

* Please review the disclaimer below.

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".