1. Home
  2. Labeler Index
  3. Doctor C&c
  4. NDC Product Code: 42979-120 Hes Clean Adam

NDC 42979-120 Hes Clean Adam

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 42979-120?
  4. Hes Clean Adam 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:
42979-120
Proprietary Name:
Hes Clean Adam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Doctor C&c
Labeler Code:
42979
Product Label ID:
8f14c436-efdd-42a3-a4e9-e06a3d87beec
Start Marketing Date: [9]
03-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 42979-120-01

Package Description: 180 mL in 1 CARTON

Product Details

What is NDC 42979-120?

The NDC code 42979-120 is assigned by the FDA to the product Hes Clean Adam which is product labeled by Doctor C&c. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42979-120-01 180 ml in 1 carton . 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 Hes Clean Adam?

Directions for use:1. If following sympoms appear after use, stop using this product and consult a dermatologist:1) in case of irritations such as inflammation and swelling during usage2) in case applied skin shows the same symptoms as 1) in direct sunlight.2. Do not apply on injuries parts, malignant tumor and other abnormal parts.3. This product is only for external use and not for internal use.

Which are Hes Clean Adam UNII Codes?

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

Which are Hes Clean Adam 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".