NDC codes

FDA NDC Directory
Product NDC (as listed)43857-0580Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43857-0580Add 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
43857-0580-1438570580014385705800130 mL in 1 BOTTLE, DROPPER (43857-0580-1)Marketed from Feb 18, 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)
Scrofularoforce
Generic name (nonproprietary)
rumex crispus, xanthoxylum fraxineum, lymph node (suis), scrophularia nodosa, baryta carbonica, baryta muriatica, belladonna, calcarea carbonica, conium maculatum, helleborus niger, iodium, kali phosphoricum, lachesis mutus, natrum phosphoricum, silicea, juniperus virginiana
Active ingredients
Rumex crispus root — 3 [hp_X]/mLZanthoxylum americanum bark — 3 [hp_X]/mLSus scrofa lymph — 8 [hp_X]/mLScrophularia nodosa whole — 8 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLBarium chloride dihydrate — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLHelleborus niger root — 12 [hp_X]/mLIodine — 12 [hp_X]/mLDibasic potassium phosphate — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLSodium phosphate, Dibasic, Heptahydrate — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLJuniperus virginiana twig — 16 [hp_X]/mL
Dosage form
Liquid
Route
Oral
Labeler
BioActive Nutritional, Inc.NDC labeler code 43857
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 43857-0580_6c5dccbb-ed1b-40b8-997a-b870288ee01eSPL ID 6c5dccbb-ed1b-40b8-997a-b870288ee01eSPL set ID 737cd410-0405-41b0-b7f2-29bb20037849UNII 9N1RM2S62C, A4KL1HMZ7T, 33A7VYU29L, 7H443NUB2T, 6P669D8HQ8, EL5GJ3U77E, WQZ3G9PF0H, 2E32821G6I, Q28R5GF371, 608DGJ6815, 9679TC07X4, CI71S98N1Z, VSW71SS07I, 70WT22SF4B, ETJ7Z6XBU4, 532BCG080LUPC 0210184341824

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

N443857058001 followed by a unit qualifier and the quantity

Package 43857-0580-01. 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 constricted feeling of the chest, palpitations with anxiety, purplish hue, burning, stinging pains, inflammation of connective tissues.** **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)

About NDC 43857-0580

What is NDC 43857-0580?
43857-0580 is the product NDC for Scrofularoforce, Rumex crispus root 3 [hp_X]/mL + 15 more ingredients liquid, listed with the FDA by BioActive Nutritional, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Scrofularoforce (Rumex Crispus, Xanthoxylum Fraxineum, Lymph Node (Suis), Scrophularia Nodosa, Baryta Carbonica, Baryta Muriatica, Belladonna, Calcarea Carbonica, Conium Maculatum, Helleborus Niger, Iodium, Kali Phosphoricum, Lachesis Mutus, Natrum Phosphoricum, Silicea, Juniperus Virginiana).
What is the active ingredient?
Rumex crispus root, Zanthoxylum americanum bark, Sus scrofa lymph, Scrophularia nodosa whole, Barium carbonate, Barium chloride dihydrate, Atropa belladonna, Oyster shell calcium carbonate, Crude, Conium maculatum flowering top, Helleborus niger root, Iodine, Dibasic potassium phosphate, Lachesis muta venom, Sodium phosphate, Dibasic, Heptahydrate, Silicon dioxide, Juniperus virginiana twig.
Who is the labeler?
BioActive Nutritional, Inc., 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 Scrofularoforce?
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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