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  4. NDC Product Code: 51785-809 Skin Clearify Spot Treatment

NDC 51785-809 Skin Clearify Spot Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51785-809?
  4. Skin Clearify Spot Treatment Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
51785-809
Proprietary Name:
Skin Clearify Spot Treatment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Herbalife International Of America Inc.
Labeler Code:
51785
Product Label ID:
99fed69a-90f4-864d-e053-2995a90aca9d
Start Marketing Date: [9]
10-01-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51785-809-00

Package Description: 1 TUBE in 1 CARTON / 15 mL in 1 TUBE

Product Details

What is NDC 51785-809?

The NDC code 51785-809 is assigned by the FDA to the product Skin Clearify Spot Treatment which is product labeled by Herbalife International Of America Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51785-809-00 1 tube in 1 carton / 15 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 Skin Clearify Spot Treatment?

UsesFor the treatment of acne. Dries up acne blemishes.

Which are Skin Clearify Spot Treatment UNII Codes?

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

Which are Skin Clearify Spot Treatment 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".