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NDC 59672-1516 Drink Ease

Avena Sativa Flowering Top,Capsicum,Strychnos Nux-vomica Seed,Veratrum Album Root,And Zinc - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 59672-1516?
  5. Drink Ease Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

NDC Product Code:
59672-1516
Proprietary Name:
Drink Ease
Non-Proprietary Name: [1]
Avena Sativa Flowering Top, Capsicum, Strychnos Nux-vomica Seed, Veratrum Album Root, And Zinc
Substance Name: [2]
Avena Sativa Flowering Top; Capsicum; Strychnos Nux-vomica Seed; Veratrum Album Root; Zinc
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Miers Laboratories
    Labeler Code:
    59672
    Product Label ID:
    23317bc3-deac-4756-8f99-d08fa32fbbfc
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    01-28-2022
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Characteristics

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

    Code Structure Chart

    Product Details

    What is NDC 59672-1516?

    The NDC code 59672-1516 is assigned by the FDA to the product Drink Ease which is a human over the counter drug product labeled by Miers Laboratories. The generic name of Drink Ease is avena sativa flowering top, capsicum, strychnos nux-vomica seed, veratrum album root, and zinc. The product's dosage form is tablet and is administered via oral form. The product is distributed in a single package with assigned NDC code 59672-1516-1 2 blister pack in 1 box / 16 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. Best taken separately from meals.

    What are Drink Ease Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
    • AVENA SATIVA FLOWERING TOP 30 [hp_C]/1
    • CAPSICUM 30 [hp_C]/1 - A plant genus of the family SOLANACEAE. The hot peppers yield CAPSAICIN, which activates VANILLOID RECEPTORS. Several varieties have sweet or pungent edible fruits that are used as vegetables when fresh and spices when the pods are dried.
    • STRYCHNOS NUX-VOMICA SEED 30 [hp_C]/1
    • VERATRUM ALBUM ROOT 30 [hp_C]/1
    • ZINC 30 [hp_C]/1 - A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.

    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

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

    [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".