BioTox Bac
- Product NDC
- 50181-0078
- 11-digit product format
- 501810078
- Labeler code
- 50181
- Product ID
- 50181-0078_11230476-2e97-4248-a7da-be620decae45
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- 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
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- The Wellness Center for Research and Education, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2021-11-08
- Marketing end
- 2026-12-09
- Substance
- CANDIDA ALBICANS; ESCHERICHIA COLI; LEGIONELLA PNEUMOPHILA; MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS; MYCOPLASMA PNEUMONIAE; PASTEURELLA MULTOCIDA; PHYTOLACCA AMERICANA ROOT; PROTEUS INCONSTANS; SHIGELLA SONNEI; STREPTOCOCCUS PNEUMONIAE; THUJA OCCIDENTALIS LEAFY TWIG
- Active strength
- 15; 15; 15; 15; 9; 15; 6; 12; 15; 15; 15 [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BioTox Bac
- Brand name suffix
- 3
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CANDIDA ALBICANS | 15 [hp_X]/mL |
| ESCHERICHIA COLI | 15 [hp_X]/mL |
| LEGIONELLA PNEUMOPHILA | 15 [hp_C]/mL |
| MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS | 15 [hp_X]/mL |
| MYCOPLASMA PNEUMONIAE | 9 [hp_X]/mL |
| PASTEURELLA MULTOCIDA | 15 [hp_X]/mL |
| PHYTOLACCA AMERICANA ROOT | 6 [hp_C]/mL |
| PROTEUS INCONSTANS | 12 [hp_X]/mL |
| SHIGELLA SONNEI | 15 [hp_C]/mL |
| STREPTOCOCCUS PNEUMONIAE | 15 [hp_X]/mL |
| THUJA OCCIDENTALIS LEAFY TWIG | 15 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4D7G21HDBC, 514B9K0L10, TJR6ZFY0F0, XH0F4IP2RX, JQE470FAD0, IX56B2GQX6, 11E6VI8VEG, UTX536WN6N, OO358E3009, BT6U234YR2, 1NT28V9397 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50181-0078-1 | BioTox Bac3 | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50181-0078 | 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) LIQUID [THE WELLNESS CENTER FOR RESEARCH AND EDUCATION, INC.] | 1 | Current NDC, Legacy NDC, 1 package rows | 20211109_29f1cba2-0bb6-43bf-a630-afc8fcb1ec81.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50181-0078-1 | 50181007801 | 30 mL in 1 BOTTLE, DROPPER (50181-0078-1) | 30 ml | 2021-11-08 | 2026-12-09 | No | No | Current |