What is NDC 50181-0082?

50181-0082 is the product NDC for BioTox Dental Foci Repair, Arnica montana whole 3 [hp_C]/mL + 9 more ingredients spray, listed with the FDA by The Wellness Center For Research and Education. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

BioTox Dental Foci Repair (Arnica Montana, Hypericum Perforatum, Plantago Major, Aconitum Napellus, Mercurius Solubilis, Hekla Lava, Argentum Nitricum, Belladonna, Hepar Sulphuris Calcareum, Silicea).

What is the active ingredient?

Arnica montana whole, Hypericum perforatum whole, Plantago major whole, Aconitum napellus whole, Mercurius solubilis, Hekla lava, Silver nitrate, Atropa belladonna, Calcium sulfide, Silicon dioxide.

The Wellness Center For Research and Education, NDC labeler code 50181. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for BioTox Dental Foci Repair?

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.

BioTox Dental Foci Repair NDC 50181-0082

NDC codes

FDA NDC Directory

Product NDC (as listed)50181-0082Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50181-0082Add 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
50181-0082-1	5018100820150181008201	30 mL in 1 BOTTLE, SPRAY (50181-0082-1)Marketed from Feb 14, 2022

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): BioTox Dental Foci Repair
Generic name (nonproprietary): arnica montana, hypericum perforatum, plantago major, aconitum napellus, mercurius solubilis, hekla lava, argentum nitricum, belladonna, hepar sulphuris calcareum, silicea
Active ingredients: Arnica montana whole — 3 [hp_C]/mLHypericum perforatum whole — 3 [hp_C]/mLPlantago major whole — 3 [hp_C]/mLAconitum napellus whole — 4 [hp_C]/mLMercurius solubilis — 4 [hp_C]/mLHekla lava — 6 [hp_C]/mLSilver nitrate — 6 [hp_C]/mLAtropa belladonna — 6 [hp_C]/mLCalcium sulfide — 6 [hp_C]/mLSilicon dioxide — 6 [hp_C]/mL
Dosage form: Spray
Route: Oral
Labeler: The Wellness Center For Research and EducationNDC labeler code 50181
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 14, 2022
Marketing end: Mar 4, 2027
Identifiers: Product ID 50181-0082_ccb14ecf-89db-4afb-a89c-263c28afa851SPL ID ccb14ecf-89db-4afb-a89c-263c28afa851SPL set ID 767f8dd2-759f-4662-9b5c-b8832309363dUNII O80TY208ZW, XK4IUX8MNB, W2469WNO6U, U0NQ8555JD, 324Y4038G2, C21158IIRK, 95IT3W8JZE, WQZ3G9PF0H, 1MBW07J51Q, ETJ7Z6XBU4UPC 0689908499996

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

N450181008201 followed by a unit qualifier and the quantity

Package 50181-0082-01. 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 Jun 6, 2025.

Indications (excerpt from the label)

INDICATIONS: For Temporary relief from right-sided tooth discomfort, dental abscess, tooth decay, loose teeth, nerve pain and general oral discomfort, Supports the body's natural slowing of excess bleeding. Promotes healthy gums.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50181-0082

What is NDC 50181-0082?: 50181-0082 is the product NDC for BioTox Dental Foci Repair, Arnica montana whole 3 [hp_C]/mL + 9 more ingredients spray, listed with the FDA by The Wellness Center For Research and Education. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: BioTox Dental Foci Repair (Arnica Montana, Hypericum Perforatum, Plantago Major, Aconitum Napellus, Mercurius Solubilis, Hekla Lava, Argentum Nitricum, Belladonna, Hepar Sulphuris Calcareum, Silicea).
What is the active ingredient?: Arnica montana whole, Hypericum perforatum whole, Plantago major whole, Aconitum napellus whole, Mercurius solubilis, Hekla lava, Silver nitrate, Atropa belladonna, Calcium sulfide, Silicon dioxide.
Who is the labeler?: The Wellness Center For Research and Education, NDC labeler code 50181. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for BioTox Dental Foci Repair?: 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.