Respiforce F-HP NDC 43857-0609

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0609Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0609Add 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
43857-0609-1	43857060901	30 mL in 1 BOTTLE, DROPPER (43857-0609-1)Marketed from Jul 23, 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): Respiforce F-HPSuffix: F-HP
Generic name (nonproprietary): aconitum napellus, arsenicum album, belladonna, bryonia (alba), eupatorium perfoliatum, ferrum phosphoricum, gelsemium sempervirens
Active ingredients: Aconitum napellus whole — 30 [hp_X]/mLArsenic trioxide — 30 [hp_X]/mLAtropa belladonna — 30 [hp_X]/mLBryonia alba root — 30 [hp_X]/mLEupatorium perfoliatum flowering top — 30 [hp_X]/mLFerrosoferric phosphate — 30 [hp_X]/mLGelsemium sempervirens root — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 23, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 43857-0609_75a1aff8-435f-4367-a5d4-c0b3cba0e849SPL ID 75a1aff8-435f-4367-a5d4-c0b3cba0e849SPL set ID a507329a-acd6-4a1e-bf8a-0223339129e7UNII U0NQ8555JD, S7V92P67HO, WQZ3G9PF0H, T7J046YI2B, 1W0775VX6E, 91GQH8I5F7, 639KR60Q1Q

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

N443857060901 followed by a unit qualifier and the quantity

Package 43857-0609-01. 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 Sep 12, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of symptoms due to influenza.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)