Dr. Talbots Mucus Cold Relief Liquid
NDC 70797-313

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 70797-313?
  4. Dr. Talbots Mucus Cold Relief Uses
  5. Active Ingredients
  6. Pharmacologic Classes

Product Information

Dr. Talbots Mucus Cold Relief (eupatorium perf, hepar sulphuris calcareum, kali bichromicum, marrubium vulgare, phosphorus, pulsatilla, rumex crispus, sambucus nigra, calcarea sulphurica, ferrum phosphoricum, kali muriaticum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Talbot's Pharmaceuticals Family Products, Llc.. This medication is typically used as a blood coagulation factor [epc]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 70797-313 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
70797-313
Proprietary Name:
Dr. Talbots Mucus Cold Relief
Non-Proprietary Name: [1]
Eupatorium Perf, Hepar Sulphuris Calcareum, Kali Bichromicum, Marrubium Vulgare, Phosphorus, Pulsatilla, Rumex Crispus, Sambucus Nigra, Calcarea Sulphurica, Ferrum Phosphoricum, Kali Muriaticum
Substance Name: [2]
Anemone Pulsatilla; Calcium Sulfate Anhydrous; Calcium Sulfide; Eupatorium Perfoliatum Flowering Top; Ferrosoferric Phosphate; Marrubium Vulgare; Phosphorus; Potassium Chloride; Potassium Dichromate; Rumex Crispus Root; Sambucus Nigra Flowering Top
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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 & Regulatory Data

Labeler Name: [5]
Talbot's Pharmaceuticals Family Products, Llc.
Labeler Code:
70797
Product Label ID:
91c311b2-a22c-0db0-e053-2995a90af3ef
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
07-20-2020
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 70797-313?

The NDC code 70797-313 is assigned by the FDA to the product Dr. Talbots Mucus Cold Relief. It is commonly known by its generic name, eupatorium perf, hepar sulphuris calcareum, kali bichromicum, marrubium vulgare, phosphorus, pulsatilla, rumex crispus, sambucus nigra, calcarea sulphurica, ferrum phosphoricum, kali muriaticum. This pharmaceutical product is labeled by Talbot's Pharmaceuticals Family Products, Llc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 70797-313-01. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

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 Active Ingredients of this product?

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.

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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".