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  4. NDC Product Code: 0395-9111 Humco Calagesic

NDC 0395-9111 Humco Calagesic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 0395-9111?
  4. Humco Calagesic 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:
0395-9111
Proprietary Name:
Humco Calagesic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Humco Holding Group, Inc.
Labeler Code:
0395
Product Label ID:
60530c40-c34d-5abf-e053-2991aa0a8eaf
Start Marketing Date: [9]
03-25-1998
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 0395-9111?

The NDC code 0395-9111 is assigned by the FDA to the product Humco Calagesic which is product labeled by Humco Holding Group, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0395-9111-96 177 ml in 1 bottle, plastic . 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 Humco Calagesic?

Adults and children 2 yr. of age and older. Shake well before using. Cleanse the skin with soap and water and let dry. Apply to the affected area using cotton or soft cloth, not more than 3 to 4 times daily as needed for comfort.Children under 2 yrs. of age. Consult a doctor before use.

Which are Humco Calagesic UNII Codes?

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

Which are Humco Calagesic 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 Humco Calagesic?

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:
  • RxCUI: 1234532 - calamine 8 % / pramoxine HCl 1 % Topical Lotion
  • RxCUI: 1234532 - calamine 80 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Lotion
  • RxCUI: 1234532 - calamine 8 % / pramoxine hydrochloride 1 % Topical Lotion
  • RxCUI: 1234539 - CALAGESIC 8 % / 1 % Topical Lotion
  • RxCUI: 1234539 - calamine 80 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Lotion [Calagesic]

* 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".