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  4. NDC Product Code: 43689-0018 Sleep Assist

NDC 43689-0018 Sleep Assist

Chamomilla,Coffea Cruda,Avena Sativa,Nux Vomica,Passiflora Incarnata Tablet, Orally - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 43689-0018?
  5. Sleep Assist Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

NDC Product Code:
43689-0018
Proprietary Name:
Sleep Assist
Non-Proprietary Name: [1]
Chamomilla, Coffea Cruda, Avena Sativa, Nux Vomica, Passiflora Incarnata
Substance Name: [2]
Arabica Coffee Bean; Avena Sativa Flowering Top; Matricaria Chamomilla Whole; Passiflora Incarnata Flowering Top; Strychnos Nux-vomica Seed
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet, Orally Disintegrating - A solid dosage form containing medicinal substances which disintegrates rapidly, usually within a matter of seconds, when placed upon the tongue.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    The Magni Company
    Labeler Code:
    43689
    Product Label ID:
    a7e428d3-9460-48d0-9c8d-1e8846bec857
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    06-19-2023
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Characteristics

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

    Code Structure Chart

    Product Details

    What is NDC 43689-0018?

    The NDC code 43689-0018 is assigned by the FDA to the product Sleep Assist which is a human over the counter drug product labeled by The Magni Company. The generic name of Sleep Assist is chamomilla, coffea cruda, avena sativa, nux vomica, passiflora incarnata. The product's dosage form is tablet, orally disintegrating and is administered via oral form. The product is distributed in a single package with assigned NDC code 43689-0018-2 1 bottle in 1 carton / 125 tablet, orally disintegrating in 1 bottle (43689-0018-1). 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 Sleep Assist?

    • Adults and children 12 years and above, dissolve 1 to 3 tablets under tongue 1/2 to 1 hour before bedtime.• Children under 12 years, consult a physician.

    What are Sleep Assist 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.

    Which are Sleep Assist UNII Codes?

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

    • MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)
    • MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (Active Moiety)
    • ARABICA COFFEE BEAN (UNII: 3SW678MX72)
    • ARABICA COFFEE BEAN (UNII: 3SW678MX72) (Active Moiety)
    • AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
    • AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
    • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
    • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
    • PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O)
    • PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (Active Moiety)

    Which are Sleep Assist 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:

    * Please review the disclaimer below.

    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".