What is NDC 70797-313?

70797-313 is the product NDC for Dr. Talbots Mucus Cold Relief, Eupatorium perfoliatum flowering top 12 [hp_X]/118mL + 10 more ingredients liquid, listed with the FDA by Talbot's Pharmaceuticals Family Products, LLC.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

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).

What is the active ingredient?

Eupatorium perfoliatum flowering top, Sambucus nigra flowering top, Calcium sulfate anhydrous, Potassium chloride, Marrubium vulgare, Phosphorus, Rumex crispus root, Ferrosoferric phosphate, Calcium sulfide, Potassium dichromate, Anemone pulsatilla.

Talbot's Pharmaceuticals Family Products, LLC., NDC labeler code 70797. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Dr. Talbots Mucus Cold Relief?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Dr. Talbots Mucus Cold Relief NDC 70797-313

NDC codes

FDA NDC Directory

Product NDC (as listed)70797-313Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70797-0313Add 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
70797-313-01	7079703130170797031301	1 BOTTLE in 1 CARTON (70797-313-01) / 118 mL in 1 BOTTLE (70797-313-04)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 Mucus Cold Relief
Generic name (nonproprietary): eupatorium perf, hepar sulphuris calcareum, kali bichromicum, marrubium vulgare, phosphorus, pulsatilla, rumex crispus, sambucus nigra, calcarea sulphurica, ferrum phosphoricum, kali muriaticum
Active ingredients: Eupatorium perfoliatum flowering top — 12 [hp_X]/118mLSambucus nigra flowering top — 12 [hp_X]/118mLCalcium sulfate anhydrous — 12 [hp_X]/118mLPotassium chloride — 6 [hp_X]/118mLMarrubium vulgare — 12 [hp_X]/118mLPhosphorus — 30 [hp_X]/118mLRumex crispus root — 12 [hp_X]/118mLFerrosoferric phosphate — 12 [hp_X]/118mLCalcium sulfide — 12 [hp_X]/118mLPotassium dichromate — 12 [hp_X]/118mLAnemone pulsatilla — 12 [hp_X]/118mL
Dosage form: Liquid
Route: Oral
Labeler: Talbot's Pharmaceuticals Family Products, LLC.NDC labeler code 70797
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 20, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 70797-313_cda11a45-601a-dbac-e053-2a95a90a2c1bSPL ID cda11a45-601a-dbac-e053-2a95a90a2c1bSPL set ID 91c311b2-a22c-0db0-e053-2995a90af3efUNII 1W0775VX6E, CT03BSA18U, E934B3V59H, 660YQ98I10, 7A72MUN24Z, 27YLU75U4W, 9N1RM2S62C, 91GQH8I5F7, 1MBW07J51Q, T4423S18FM, I76KB35JEVUPC 0370797300035
Pharmacologic class: Blood Coagulation Factor; 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

N470797031301 followed by a unit qualifier and the quantity

Package 70797-0313-01. 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

Current FDA label (SPL), effective Oct 5, 2021.

Indications (excerpt from the label)

Uses Uses Temporarily relieves mucusy cough cough and congestion associated with colds nasal and sinus congestion mucus in chest sneezing runny nose Indication

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70797-313

What is NDC 70797-313?: 70797-313 is the product NDC for Dr. Talbots Mucus Cold Relief, Eupatorium perfoliatum flowering top 12 [hp_X]/118mL + 10 more ingredients liquid, listed with the FDA by Talbot's Pharmaceuticals Family Products, LLC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: 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).
What is the active ingredient?: Eupatorium perfoliatum flowering top, Sambucus nigra flowering top, Calcium sulfate anhydrous, Potassium chloride, Marrubium vulgare, Phosphorus, Rumex crispus root, Ferrosoferric phosphate, Calcium sulfide, Potassium dichromate, Anemone pulsatilla.
Who is the labeler?: Talbot's Pharmaceuticals Family Products, LLC., NDC labeler code 70797. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dr. Talbots Mucus Cold Relief?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.