NDC 59672-0532 Drink Ease

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:
59672-0532
Proprietary Name:
Drink Ease
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lc Industries
Labeler Code:
59672
Start Marketing Date: [9]
04-05-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
9 MM
Imprint(s):
ML
Score:
1

Product Packages

NDC Code 59672-0532-1

Package Description: 32 TABLET in 1 BLISTER PACK

Product Details

What is NDC 59672-0532?

The NDC code 59672-0532 is assigned by the FDA to the product Drink Ease which is product labeled by Lc Industries. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59672-0532-1 32 tablet in 1 blister pack . 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 Drink Ease?

AgeDoseAdultsChew one tablet with a large glass of water at bedtime after drinking alcohol. Repeat every two hours if necessary. However variation of these directions is acceptable and may be preferable. Best taken separately from meals.

Which are Drink Ease UNII Codes?

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

Which are Drink Ease 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".