Bacterial Immune Stimulator Liquid
NDC Package 63083-6006-2
Package Information
Bacterial Immune Stimulator liquids is temporarily reduces occasional mild abdominal pain or discomfort, nausea, headache, fatigue, runny nose, chills, or cough.*. This formulation utilizes a liquid delivery system. Marketed by Professional Complementary Health Formulas, this product is identified by NDC 63083-6006.
Identification & Billing
Clinical Specifications
- ALOE 6 [hp_X]/59mL
- CALCIUM SULFIDE 30 [hp_X]/59mL
- GOLDENSEAL 30 [hp_X]/59mL
- SULFUR 6 [hp_X]/59mL
- GARLIC 30 [hp_X]/59mL
- GRAPHITE 30 [hp_X]/59mL
- ESCHERICHIA COLI 30 [hp_X]/59mL
- RANCID BEEF 30 [hp_X]/59mL
- BACILLUS ANTHRACIS IMMUNOSERUM RABBIT 30 [hp_X]/59mL
- DELPHINIUM STAPHISAGRIA SEED 30 [hp_X]/59mL
- DIPHTHERIAL RESPIRATORY PSEUDOMEMBRANE HUMAN 30 [hp_X]/59mL
- STREPTOCOCCUS PYOGENES 12 [hp_X]/59mL
- STAPHYLOCOCCUS AUREUS 6 [hp_X]/59mL
- TREPONEMIC SKIN CANKER HUMAN 12 [hp_X]/59mL
- CLOSTRIDIUM BOTULINUM 30 [hp_X]/59mL
- BOVINE TUBERCULIN 30 [hp_X]/59mL
- EUCALYPTOL 30 [hp_X]/59mL
- CANIS LUPUS FAMILIARIS MILK 6 [hp_X]/59mL
- COW MILK 30 [hp_X]/59mL
Regulatory & Marketing
Hierarchy Structure
- 63083 - Professional Complementary Health Formulas
- 63083-6006 - Bacterial Immune Stimulator
- 63083-6006-2 - 59 mL in 1 BOTTLE, DROPPER
- 63083-6006 - Bacterial Immune Stimulator
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 63083-6006-2 identifies a specific commercial package of 59 ml in 1 bottle, dropper of Bacterial Immune Stimulator 6006, a human over the counter drug labeled by Professional Complementary Health Formulas. This liquid is formulated for oral use and contains aloe; calcium sulfide; goldenseal; sulfur; garlic; graphite; escherichia coli; rancid beef; bacillus anthracis immunoserum rabbit; delphinium staphisagria seed; diphtherial respiratory pseudomembrane human; streptococcus pyogenes; staphylococcus aureus; treponemic skin canker human; clostridium botulinum; bovine tuberculin; eucalyptol; canis lupus familiaris milk; cow milk as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Professional Complementary Health Formulas on August 15, 1984. The current certification is valid through December 31, 2027.
How is this Professional Complementary Health Formulas product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 63083600602. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.