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  4. NDC Product Code: 65588-2210 Maximum-h

NDC 65588-2210 Maximum-h

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 65588-2210?
  4. Maximum-h 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:
65588-2210
Proprietary Name:
Maximum-h
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
New Gpc, Inc.
Labeler Code:
65588
Product Label ID:
eb9bf7f3-172b-40fb-93d3-cb4c633b3506
Start Marketing Date: [9]
12-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 65588-2210?

The NDC code 65588-2210 is assigned by the FDA to the product Maximum-h which is product labeled by New Gpc, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 65588-2210-1 1 tube in 1 carton / 20 g in 1 tube, 65588-2210-2 1 tube in 1 carton / 40 g 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 Maximum-h?

Adults and Children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.Children under 2 years of age: Do not use, consult a Doctor.For hemorrhoids - clean affected area with a cleansing wipe, then dry with a soft cloth. Apply externally to lower part of anal canal only. Apply up to 3 times daily at night and after every bowel movement.

Which are Maximum-h UNII Codes?

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

Which are Maximum-h 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 Maximum-h?

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".