BioTox P
- Product NDC
- 50181-0057
- 11-digit product format
- 501810057
- Labeler code
- 50181
- Product ID
- 50181-0057_24ce3717-7660-4140-b48a-29587e097278
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pertussinum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- The Wellness Center For Research and Education
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-02-27
- Marketing end
- 0000-00-00
- Substance
- HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED
- Active strength
- 15 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50181-0057 | BIOTOX P (PERTUSSINUM) LIQUID [THE WELLNESS CENTER FOR RESEARCH AND EDUCATION] | 1 | Legacy NDC | 20180228_bd1a67b8-035d-4a3e-b74f-9b63de30c834.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50181-0057-1 | 50181005701 | 30 mL in 1 BOTTLE, DROPPER (50181-0057-1) | 30 ml | 2018-02-27 | 0000-00-00 | No | No | Current |