Pertussinum is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Human Sputum, Bordetella Pertussis Infected.
Product ID | 71919-527_7e5a29dd-8a6e-95a1-e053-2991aa0a2316 |
NDC | 71919-527 |
Product Type | Human Otc Drug |
Proprietary Name | Pertussinum |
Generic Name | Human Sputum, Bordetella Pertussis Infected |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2009-02-04 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Washington Homeopathic Products |
Substance Name | HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED |
Active Ingredient Strength | 30 [hp_C]/mL |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2009-02-04 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-02-04 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-02-04 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-02-04 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-02-04 |
Ingredient | Strength |
---|---|
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED | 30 [hp_C]/mL |
SPL SET ID: | 266174d5-4c5e-4cb6-bfc9-e33ace04263a |
Manufacturer | |
UNII | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0220-3968 | Pertussinum | HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED |
55714-9011 | Pertussinum | Pertussinum |
71919-527 | Pertussinum | HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED |
50181-0057 | BioTox P | Pertussinum |