Respitory Tonic F NDC 43857-0583

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0583Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0583Add 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
43857-0583-1	43857058301	60 mL in 1 BOTTLE, DROPPER (43857-0583-1)Marketed from May 10, 2021

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Respitory Tonic F
Generic name (nonproprietary): echinacea (angustifolia), uva-ursi, baptisia tinctoria, convallaria majalis, kali muriaticum, pinus sylvestris, thuja occidentalis, bryonia (alba), condurango, crotalus horridus, ginkgo biloba, lachesis mutus, selenium metallicum, tabebuia impetiginosa, viscum album
Active ingredients: Echinacea angustifolia whole — 1 [hp_X]/mLArctostaphylos uva-ursi leaf — 1 [hp_X]/mLBaptisia tinctoria root — 3 [hp_X]/mLConvallaria majalis — 6 [hp_X]/mLPotassium chloride — 6 [hp_X]/mLPinus sylvestris leafy twig — 6 [hp_X]/mLThuja occidentalis leafy twig — 6 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLMarsdenia condurango bark — 12 [hp_X]/mLCrotalus horridus horridus venom — 12 [hp_X]/mLGinkgo — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLTabebuia impetiginosa bark — 12 [hp_X]/mLViscum album fruiting top — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 10, 2021
Listing expires: Dec 31, 2027
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 43857-0583_1fcd3d4a-a24d-41d0-ba2b-4827c04e7c69SPL ID 1fcd3d4a-a24d-41d0-ba2b-4827c04e7c69SPL set ID 17684967-1e3c-4776-9ae9-d43fa1ebebb1UNII VB06AV5US8, 3M5V3D1X36, 5EF0HWI5WU, QHH4HVF5QE, 660YQ98I10, Q1RGP4UB73, 1NT28V9397, T7J046YI2B, YHA2XLJ956, 19FUJ2C58T, VSW71SS07I, H6241UJ22B, 6GLA1946WX, BK9092J5MPUPC 0210184341275
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

N443857058301 followed by a unit qualifier and the quantity

Package 43857-0583-01. 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 Mar 9, 2026.

Indications (excerpt from the label)

USES: For temporary relief of various strains of influenza.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)