What is NDC 44911-0464?

44911-0464 is the product NDC for Free Radistat, Baptisia tinctoria root 3 [hp_X]/mL + 12 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Free Radistat (Baptisia Tinctoria, Echinacea (Angustifolia), Fucus Vesiculosus, Uva-Ursi, Phytolacca Decandra, Arsenicum Album, Aurum Metallicum, Ferrum Phosphoricum, Iodium, Iridium Metallicum, Lachesis Mutus, Zincum Metallicum, Cadmium Sulphuratum).

What is the active ingredient?

Baptisia tinctoria root, Echinacea angustifolia whole, Fucus vesiculosus, Arctostaphylos uva-ursi leaf, Phytolacca americana root, Arsenic trioxide, Gold, Ferrosoferric phosphate, Iodine, Iridium, Lachesis muta venom, Zinc, Cadmium sulfide.

Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Free Radistat?

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.

Free Radistat NDC 44911-0464 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0464Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0464Add 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
44911-0464-1	4491104640144911046401	30 mL in 1 BOTTLE, DROPPER (44911-0464-1)Marketed from Aug 17, 2018

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): Free Radistat
Generic name (nonproprietary): baptisia tinctoria, echinacea (angustifolia), fucus vesiculosus, uva-ursi, phytolacca decandra, arsenicum album, aurum metallicum, ferrum phosphoricum, iodium, iridium metallicum, lachesis mutus, zincum metallicum, cadmium sulphuratum
Active ingredients: Baptisia tinctoria root — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLFucus vesiculosus — 3 [hp_X]/mLArctostaphylos uva-ursi leaf — 3 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLGold — 12 [hp_X]/mLFerrosoferric phosphate — 12 [hp_X]/mLIodine — 12 [hp_X]/mLIridium — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLZinc — 12 [hp_X]/mLCadmium sulfide — 13 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.NDC labeler code 44911
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 17, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 44911-0464_2f7a7bae-4ee1-482a-a7f6-ed233a4efba2SPL ID 2f7a7bae-4ee1-482a-a7f6-ed233a4efba2SPL set ID 1427d5af-497b-4585-aba9-3a8fdcd7745cUNII 5EF0HWI5WU, VB06AV5US8, 535G2ABX9M, 3M5V3D1X36, 11E6VI8VEG, S7V92P67HO, 79Y1949PYO, 91GQH8I5F7, 9679TC07X4, 44448S9773, VSW71SS07I, J41CSQ7QDS, 057EZR4Z7Q
Pharmacologic class: Standardized Chemical Allergen

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

N444911046401 followed by a unit qualifier and the quantity

Package 44911-0464-01. 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 Apr 22, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve weakness, tiredness, and general exhaustion.** **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 44911-0464

What is NDC 44911-0464?: 44911-0464 is the product NDC for Free Radistat, Baptisia tinctoria root 3 [hp_X]/mL + 12 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Free Radistat (Baptisia Tinctoria, Echinacea (Angustifolia), Fucus Vesiculosus, Uva-Ursi, Phytolacca Decandra, Arsenicum Album, Aurum Metallicum, Ferrum Phosphoricum, Iodium, Iridium Metallicum, Lachesis Mutus, Zincum Metallicum, Cadmium Sulphuratum).
What is the active ingredient?: Baptisia tinctoria root, Echinacea angustifolia whole, Fucus vesiculosus, Arctostaphylos uva-ursi leaf, Phytolacca americana root, Arsenic trioxide, Gold, Ferrosoferric phosphate, Iodine, Iridium, Lachesis muta venom, Zinc, Cadmium sulfide.
Who is the labeler?: Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Free Radistat?: 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.