What is NDC 50181-0078?

50181-0078 is the product NDC for BioTox Bac 3, Mycoplasma pneumoniae 9 [hp_X]/mL + 10 more ingredients liquid, listed with the FDA by The Wellness Center for Research and Education, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

BioTox Bac 3 (Mycoplasma Pneumoniae, Proteus (Vulgaris), Candida Albicans, Colibacillinum Cum Natrum Muriaticum, Mycobacterium Paratuberculosis, Pasteurellosis (Pasteurella Multocida), Pneumococcinum, Thuja Occidentalis, Mycobacterium Avium Paratuberculosis, Phytolacca Decandra, Legionella Pneumophila, Shigella Sonnei).

What is the active ingredient?

Mycoplasma pneumoniae, Proteus inconstans, Candida albicans, Escherichia coli, Mycobacterium avium subsp. Paratuberculosis, Pasteurella multocida, Streptococcus pneumoniae, Thuja occidentalis leafy twig, Phytolacca americana root, Legionella pneumophila, Shigella sonnei.

The Wellness Center for Research and Education, Inc., 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 Bac 3?

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 Bac 3 NDC 50181-0078 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50181-0078Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50181-0078Add 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
50181-0078-1	5018100780150181007801	30 mL in 1 BOTTLE, DROPPER (50181-0078-1)Marketed from Nov 8, 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): BioTox Bac 3Suffix: 3
Generic name (nonproprietary): mycoplasma pneumoniae, proteus (vulgaris), candida albicans, colibacillinum cum natrum muriaticum, mycobacterium paratuberculosis, pasteurellosis (pasteurella multocida), pneumococcinum, thuja occidentalis, mycobacterium avium paratuberculosis, phytolacca decandra, legionella pneumophila, shigella sonnei
Active ingredients: Mycoplasma pneumoniae — 9 [hp_X]/mLProteus inconstans — 12 [hp_X]/mLCandida albicans — 15 [hp_X]/mLEscherichia coli — 15 [hp_X]/mLMycobacterium avium subsp. Paratuberculosis — 15 [hp_X]/mLPasteurella multocida — 15 [hp_X]/mLStreptococcus pneumoniae — 15 [hp_X]/mLThuja occidentalis leafy twig — 15 [hp_X]/mLPhytolacca americana root — 6 [hp_C]/mLLegionella pneumophila — 15 [hp_C]/mLShigella sonnei — 15 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: The Wellness Center for Research and Education, Inc.NDC labeler code 50181
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 8, 2021
Marketing end: Dec 9, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 50181-0078_11230476-2e97-4248-a7da-be620decae45SPL ID 11230476-2e97-4248-a7da-be620decae45SPL set ID 29f1cba2-0bb6-43bf-a630-afc8fcb1ec81UNII JQE470FAD0, UTX536WN6N, 4D7G21HDBC, 514B9K0L10, XH0F4IP2RX, IX56B2GQX6, BT6U234YR2, 1NT28V9397, 11E6VI8VEG, TJR6ZFY0F0, OO358E3009UPC 0737278069025
Pharmacologic class: Non-Standardized Fungal 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

N450181007801 followed by a unit qualifier and the quantity

Package 50181-0078-01. 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 of fever and chills. Promotes a productive wet cough and the coughing up of phlegm. expectorant. Helps relieve the presence of mucus in the stool and loose stools.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50181-0078

What is NDC 50181-0078?: 50181-0078 is the product NDC for BioTox Bac 3, Mycoplasma pneumoniae 9 [hp_X]/mL + 10 more ingredients liquid, listed with the FDA by The Wellness Center for Research and Education, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: BioTox Bac 3 (Mycoplasma Pneumoniae, Proteus (Vulgaris), Candida Albicans, Colibacillinum Cum Natrum Muriaticum, Mycobacterium Paratuberculosis, Pasteurellosis (Pasteurella Multocida), Pneumococcinum, Thuja Occidentalis, Mycobacterium Avium Paratuberculosis, Phytolacca Decandra, Legionella Pneumophila, Shigella Sonnei).
What is the active ingredient?: Mycoplasma pneumoniae, Proteus inconstans, Candida albicans, Escherichia coli, Mycobacterium avium subsp. Paratuberculosis, Pasteurella multocida, Streptococcus pneumoniae, Thuja occidentalis leafy twig, Phytolacca americana root, Legionella pneumophila, Shigella sonnei.
Who is the labeler?: The Wellness Center for Research and Education, Inc., 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 Bac 3?: 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.