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  4. NDC Product Code: 70797-312 Dr. Talbots Daily Allergy Relief

NDC 70797-312 Dr. Talbots Daily Allergy Relief

Allium Cepa,Aralia Racemosa,Euphrasia Officinalis,Galphimia Glauca,Histaminum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70797-312?
  4. Dr. Talbots Daily Allergy Relief Uses
  5. Active Ingredients
  6. Pharmacologic Classes

Product Information

NDC Product Code:
70797-312
Proprietary Name:
Dr. Talbots Daily Allergy Relief
Non-Proprietary Name: [1]
Allium Cepa, Aralia Racemosa, Euphrasia Officinalis, Galphimia Glauca, Histaminum Hydrochloricum, Luffa Operculata, Pulsatilla, Solidago, Natrum Muriaticum
Substance Name: [2]
Anemone Pulsatilla; Aralia Racemosa Root; Euphrasia Stricta; Galphimia Glauca Flowering Top; Histamine Dihydrochloride; Luffa Operculata Fruit; Onion; Sodium Chloride; Solidago Virgaurea Flowering Top
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Talbot's Pharmaceuticals Family Products, Llc.
    Labeler Code:
    70797
    Product Label ID:
    91c2795d-4cde-6e2c-e053-2995a90a0096
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    07-20-2020
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 70797-312?

    The NDC code 70797-312 is assigned by the FDA to the product Dr. Talbots Daily Allergy Relief which is a human over the counter drug product labeled by Talbot's Pharmaceuticals Family Products, Llc.. The generic name of Dr. Talbots Daily Allergy Relief is allium cepa, aralia racemosa, euphrasia officinalis, galphimia glauca, histaminum hydrochloricum, luffa operculata, pulsatilla, solidago, natrum muriaticum. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 70797-312-01 1 bottle in 1 carton / 118 ml in 1 bottle (70797-312-04). 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 Dr. Talbots Daily Allergy Relief?

    Shake before use, natural juice may settleMeasure only with the dosing syringe providedDo not use dosing syringe with other productsOn dosing syringe, weight is specific to productOn dosing syringe, ml = milliliter, lbs = pounds, kgs = kilogramsChildren under 6 months of age, consult a medical professional before using this product.For sudden onset of symptoms: Use every 15 minutes for up to 8 doses until symptoms relieved, then every 2 hours thereafter.Children 6 - 18 lbs or 3 - 8 kgs 1.25 ml every 2 hours, reduce frequency when symptoms improveChildren 19 - 29 lbs or 9 - 13 kgs 2.5 ml every 2 hours, reduce frequency when symptoms improveChildren 30 - 90 lbs or 14 - 41 kgs 5 ml every 2 hours, reduce frequency when symptoms improve

    What are Dr. Talbots Daily Allergy Relief 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 the Pharmacologic Classes for Dr. Talbots Daily Allergy Relief?

    * 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".