Dr. Talbots Pain Fever Relief NDC 70797-315

NDC codes

FDA NDC Directory

Product NDC (as listed)70797-315Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70797-0315Add 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
70797-315-01	70797031501	1 BOTTLE in 1 BOTTLE (70797-315-01) / 118 mL in 1 BOTTLE (70797-315-04)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 Pain Fever Relief
Generic name (nonproprietary): calendula officinalis, chamomilla, echinacea angustifolia, eupatorium perfoliatum, hepar sulphuris calcareum, sulphur, ferrum phosphoricum, kali muriaticum
Active ingredients: Matricaria chamomilla — 12 [hp_X]/118mLEupatorium perfoliatum flowering top — 12 [hp_X]/118mLCalendula officinalis flowering top — 12 [hp_X]/118mLEchinacea angustifolia — 12 [hp_X]/118mLCalcium sulfide — 12 [hp_X]/118mLPotassium chloride — 6 [hp_X]/118mLFerrosoferric phosphate — 12 [hp_X]/118mLCosmos sulphureus flowering top — 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 70797-315_cda0f5bd-dc31-4faf-e053-2995a90ad4aeSPL ID cda0f5bd-dc31-4faf-e053-2995a90ad4aeSPL set ID 91d50391-f6a7-febf-e053-2995a90a1b02UNII G0R4UBI2ZZ, 1W0775VX6E, 18E7415PXQ, VB06AV5US8, 1MBW07J51Q, 660YQ98I10, 91GQH8I5F7, WKB165X336UPC 0370797300059
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

N470797031501 followed by a unit qualifier and the quantity

Package 70797-0315-01. 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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)