Pneumoforce NDC 43857-0551

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0551Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0551Add 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
43857-0551-1	43857055101	30 mL in 1 BOTTLE, DROPPER (43857-0551-1)Marketed from Mar 6, 2020

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): Pneumoforce
Generic name (nonproprietary): althaea officinalis, natrum carbonicum, rheum (palmatum), verbascum thapsus, zingiber officinale, aconitum napellus, drosera (rotundifolia), kali bichromicum, lobelia inflata, phosphorus
Active ingredients: Althaea officinalis root — 3 [hp_X]/mLSodium carbonate — 3 [hp_X]/mLRheum palmatum root — 3 [hp_X]/mLVerbascum thapsus whole — 3 [hp_X]/mLGinger — 3 [hp_X]/mLAconitum napellus whole — 12 [hp_X]/mLDrosera rotundifolia whole — 12 [hp_X]/mLPotassium dichromate — 12 [hp_X]/mLLobelia inflata whole — 12 [hp_X]/mLPhosphorus — 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: Mar 6, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 43857-0551_5d8cab75-287d-4e8a-b75f-a4083f481200SPL ID 5d8cab75-287d-4e8a-b75f-a4083f481200SPL set ID a58c6a1a-ad3e-4055-8077-b6738105087dUNII TRW2FUF47H, 45P3261C7T, G025DAL7CE, C9TD27U172, C5529G5JPQ, U0NQ8555JD, QR44N9XPJQ, T4423S18FM, 9PP1T3TC5U, 27YLU75U4WUPC 0210184340797
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N443857055101 followed by a unit qualifier and the quantity

Package 43857-0551-01. 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 dry hacking cough, hoarseness, bronchial congestions and hay fever symptoms, and difficulty breathing with tightness of chest from constriction of chest.** **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)