NDC codes

FDA NDC Directory
Product NDC (as listed)43857-0599Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43857-0599Add 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 NDC11-digit (billing)PackageCopy
43857-0599-1438570599014385705990130 mL in 1 BOTTLE, DROPPER (43857-0599-1)Marketed from Jun 1, 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
Generic name (nonproprietary)
arnica montana, asclepias tuberosa, eriodictyon californicum, eucalyptus globulus, lobelia inflata, plantago major, trifolium pratense, arsenicum album, belladonna, bryonia, carbo vegetabilis, grindelia, kali carbonicum, natrum sulphuricum, pulsatilla,
Active ingredients
Arnica montana whole — 3 [hp_X]/mLAsclepias tuberosa root — 3 [hp_X]/mLEriodictyon californicum leaf — 3 [hp_X]/mLEucalyptus globulus leaf — 3 [hp_X]/mLLobelia inflata whole — 3 [hp_X]/mLPlantago major whole — 3 [hp_X]/mLTrifolium pratense flower — 3 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLActivated charcoal — 12 [hp_X]/mLGrindelia hirsutula flowering top — 12 [hp_X]/mLPotassium carbonate — 12 [hp_X]/mLSodium sulfate — 12 [hp_X]/mLPulsatilla vulgaris whole — 12 [hp_X]/mL
Dosage form
Liquid
Route
Oral
Labeler
BioActive NutritionalNDC labeler code 43857
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 43857-0599_39583480-a1ae-4e26-a9be-cfe57922ebf7SPL ID 39583480-a1ae-4e26-a9be-cfe57922ebf7SPL set ID e9360698-bffb-4c91-b019-22e1e56704eeUNII O80TY208ZW, 1ZL82U5D18, 2Y7TIQ135H, S546YLW6E6, 9PP1T3TC5U, W2469WNO6U, 4JS0838828, S7V92P67HO, WQZ3G9PF0H, T7J046YI2B, 2P3VWU3H10, IDB0NAZ6AI, BQN1B9B9HA, 0YPR65R21J, I76KB35JEV

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

N443857059901 followed by a unit qualifier and the quantity

Package 43857-0599-01. 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 .

Indications (excerpt from the label)

USES: For temporary relief of tightness in the chest, and shortness of breath during damp weather.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43857-0599

What is NDC 43857-0599?
43857-0599 is the product NDC for Respiforce A, Arnica montana whole 3 [hp_X]/mL + 14 more ingredients liquid, listed with the FDA by BioActive Nutritional. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Respiforce A (Arnica montana, Asclepias tuberosa, Eriodictyon californicum, Eucalyptus globulus, Lobelia inflata, Plantago major, Trifolium pratense, Arsenicum album, Belladonna, Bryonia, Carbo vegetabilis, Grindelia, Kali carbonicum, Natrum sulphuricum, Pulsatilla,).
What is the active ingredient?
Arnica montana whole, Asclepias tuberosa root, Eriodictyon californicum leaf, Eucalyptus globulus leaf, Lobelia inflata whole, Plantago major whole, Trifolium pratense flower, Arsenic trioxide, Atropa belladonna, Bryonia alba root, Activated charcoal, Grindelia hirsutula flowering top, Potassium carbonate, Sodium sulfate, Pulsatilla vulgaris whole.
Who is the labeler?
BioActive Nutritional, NDC labeler code 43857. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Respiforce A?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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