NDC 57520-0432 Type 11 Dizziness Max

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
57520-0432
Proprietary Name:
Type 11 Dizziness Max
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Apotheca Company
Labeler Code:
57520
Start Marketing Date: [9]
07-15-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
NONE
Score:
1

Product Packages

NDC Code 57520-0432-1

Package Description: 15000 mg in 1 BOTTLE

Product Details

What is NDC 57520-0432?

The NDC code 57520-0432 is assigned by the FDA to the product Type 11 Dizziness Max which is product labeled by Apotheca Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57520-0432-1 15000 mg in 1 bottle . 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 Type 11 Dizziness Max?

This product is used as INDICATIONS:  For relief of ringing in the ear from Dizziness, Loss of Balance.

Which are Type 11 Dizziness Max UNII Codes?

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

Which are Type 11 Dizziness Max 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".