1. Home
  2. Labeler Index
  3. Perdido Key Health And Wellness Inc
  4. NDC Product Code: 70104-110 B-combo

NDC 70104-110 B-combo

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 70104-110?
  5. Active 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:
70104-110
Proprietary Name:
B-combo
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Perdido Key Health And Wellness Inc
Labeler Code:
70104
Product Label ID:
253e0d06-8a36-5175-e054-00144ff8d46c
Start Marketing Date: [9]
11-23-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 70104-110-01

Package Description: 1 mL in 1 VIAL

Product Details

What is NDC 70104-110?

The NDC code 70104-110 is assigned by the FDA to the product B-combo which is product labeled by Perdido Key Health And Wellness Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70104-110-01 1 ml in 1 vial . 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.

Which are B-combo UNII Codes?

The UNII codes for the active 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".