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NDC 61657-0970 Total Andro-bal

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 61657-0970?
  4. Total Andro-bal 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:
61657-0970
Proprietary Name:
Total Andro-bal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
White Manufacturing Inc. Dba Micro West
Labeler Code:
61657
Product Label ID:
8b3af556-74fb-4054-80ca-2a973a9bc617
Start Marketing Date: [9]
04-01-2007
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 61657-0970?

The NDC code 61657-0970 is assigned by the FDA to the product Total Andro-bal which is product labeled by White Manufacturing Inc. Dba Micro West. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61657-0970-1 30 ml in 1 bottle, pump . 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 Total Andro-bal?

DIRECTIONS: TAKE 2 PUMP SPRAYS 3 TIMES DAILY. HOLD UNDER TONGUE 30 SECONDS BEFORE SWALLOWING. MORE FREQUENT DOSAGES MAY BE USED ACCORDING TO SYMPTOMATIC NEEDS. FOR AGEWS 12 TO ADULT.

Which are Total Andro-bal UNII Codes?

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

Which are Total Andro-bal 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".