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  4. NDC Product Code: 66738-561 Jack Black Grab N Go Traveler

NDC 66738-561 Jack Black Grab N Go Traveler

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 66738-561?
  5. Jack Black Grab N Go Traveler Uses
  6. Active Ingredients UNII Codes
  7. 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:
66738-561
Proprietary Name:
Jack Black Grab N Go Traveler
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jack Black L.l.c
Labeler Code:
66738
Product Label ID:
af87281d-1fae-edf4-e053-2a95a90ae787
Start Marketing Date: [9]
09-17-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Code Structure Chart

Product Details

What is NDC 66738-561?

The NDC code 66738-561 is assigned by the FDA to the product Jack Black Grab N Go Traveler which is product labeled by Jack Black L.l.c. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66738-561-40 78 g in 1 kit . 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 Jack Black Grab N Go Traveler?

Turn base to raise product. Apply to underarm only.

Which are Jack Black Grab N Go Traveler UNII Codes?

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

  • ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE)
  • ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (Active Moiety)

Which are Jack Black Grab N Go Traveler 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".