Dr. Talbots Cough Relief NDC 70797-314

NDC codes

FDA NDC Directory

Product NDC (as listed)70797-314Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70797-0314Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
70797-314-01	70797031401	1 BOTTLE in 1 CARTON (70797-314-01) / 118 mL in 1 BOTTLE (70797-314-04)Marketed from Jul 20, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Dr. Talbots Cough Relief
Generic name (nonproprietary): antimonium tartaricum, drosera rotundifolia, ipecacuanha, phosphorus, rumex crispus, spongia tosta, sticta pulmonaria, kali sulphuricum
Active ingredients: Pulmonaria officinalis whole — 12 [hp_X]/118mLAntimony tartrate ion — 12 [hp_X]/118mLDrosera rotundifolia flowering top — 12 [hp_X]/118mLPhosphorus — 12 [hp_X]/118mLRumex crispus root — 12 [hp_X]/118mLPotassium sulfate — 6 [hp_X]/118mLSpongia officinalis skeleton, Roasted — 12 [hp_X]/118mLIpecac — 12 [hp_X]/118mL
Dosage form: Liquid
Route: Oral
Labeler: Talbot's Pharmaceuticals Family Products, LLC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 20, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 70797-314_cda0f4dc-f551-a6b7-e053-2a95a90a7745SPL ID cda0f4dc-f551-a6b7-e053-2a95a90a7745SPL set ID 91d3e4d6-356b-4e7f-e053-2a95a90a5158UNII 483B0A2Y00, CQN5KB2U1M, 75O014T1HG, 27YLU75U4W, 9N1RM2S62C, 1K573LC5TV, 1PIP394IID, 62I3C8233LUPC 0370797300042
Pharmacologic class: Osmotic Laxative; Potassium Salt

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470797031401 followed by a unit qualifier and the quantity

Package 70797-0314-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

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