Dr. Talbots Cough Relief Liquid
NDC Package 70797-314-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Dr. Talbots Cough Relief (antimonium tartaricum, drosera rotundifolia, ipecacuanha, phosphorus, rumex crispus, spongia tosta, sticta pulmonaria, kali sulphuricum) liquids is 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. This formulation utilizes a liquid delivery system. Marketed by Talbot's Pharmaceuticals Family Products, Llc., this product is identified by NDC 70797-314.

Identification & Billing

NDC Package Code
70797-314-01
Package Description
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE (70797-314-04)
Product Code
70797-314
11-Digit Billing Format
70797031401

Clinical Specifications

Proprietary Name
Dr. Talbots Cough Relief
Non-Proprietary Name
Antimonium Tartaricum, Drosera Rotundifolia, Ipecacuanha, Phosphorus, Rumex Crispus, Spongia Tosta, Sticta Pulmonaria, Kali Sulphuricum
Substance Name
Antimony Tartrate Ion; Drosera Rotundifolia Flowering Top; Ipecac; Phosphorus; Potassium Sulfate; Pulmonaria Officinalis Whole; Rumex Crispus Root; Spongia Officinalis Skeleton, Roasted
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
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

Regulatory & Marketing

Labeler Name
Talbot's Pharmaceuticals Family Products, Llc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
07-20-2020
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 70797-314-01 identifies a specific commercial package of 1 bottle in 1 carton / 118 ml in 1 bottle (70797-314-04) of Dr. Talbots Cough Relief, a human over the counter drug labeled by Talbot's Pharmaceuticals Family Products, Llc.. This liquid is formulated for oral use and contains antimony tartrate ion; drosera rotundifolia flowering top; ipecac; phosphorus; potassium sulfate; pulmonaria officinalis whole; rumex crispus root; spongia officinalis skeleton, roasted as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Talbot's Pharmaceuticals Family Products, Llc. on July 20, 2020. The current certification is valid through December 31, 2026.

How is this Talbot's Pharmaceuticals Family Products, Llc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70797031401. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
70797-314-01
11-Digit CMS (5-4-2)
70797-0314-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.