Respiforce A-HP NDC 43857-0612

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0612Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0612Add 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
43857-0612-1	43857061201	30 mL in 1 BOTTLE, DROPPER (43857-0612-1)Marketed from Sep 3, 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 A-HP
Generic name (nonproprietary): arsenicum album, belladonna, ipecacuanha, kali carbonicum, lobelia inflata, natrum sulphuricum, silicea
Active ingredients: Arsenic trioxide — 30 [hp_X]/mLAtropa belladonna — 30 [hp_X]/mLIpecac — 30 [hp_X]/mLPotassium carbonate — 30 [hp_X]/mLLobelia inflata whole — 30 [hp_X]/mLSodium sulfate — 30 [hp_X]/mLSilicon dioxide — 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: Sep 3, 2021
Listing expires: Dec 31, 2027
Identifiers: Product ID 43857-0612_f869579c-5b5b-4a5c-b98c-db6b1281a585SPL ID f869579c-5b5b-4a5c-b98c-db6b1281a585SPL set ID ebf5f0c7-e7a4-45fe-acfd-52c46a8d789cUNII S7V92P67HO, WQZ3G9PF0H, 62I3C8233L, BQN1B9B9HA, 9PP1T3TC5U, 0YPR65R21J, ETJ7Z6XBU4UPC 0810184340508

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

N443857061201 followed by a unit qualifier and the quantity

Package 43857-0612-01. 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 5, 2026.

Indications (excerpt from the label)

USES: For temporary relief of symptoms of tightness in the chest, wheezing, and difficulty breathing due to low oxygen to the lungs.** **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)