Bye, Bye Ver
- Product NDC
- 57520-0061
- 11-digit product format
- 575200061
- Labeler code
- 57520
- Product ID
- 57520-0061_172bfec6-8c6f-4d34-8df8-24dead3daf6f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Artemisia vulgaris, Filix mas, Tanacetum vulgare, Teucrium marum, Absinthium, Cina, Chenopodium anthelminticum,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Apotheca Company
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2010-02-05
- Marketing end
- 2022-11-23
- Substance
- ARTEMISIA ABSINTHIUM POLLEN; ARTEMISIA CINA FLOWER; ARTEMISIA VULGARIS ROOT; ASCARIS LUMBRICOIDES; CHENOPODIUM AMBROSIOIDES; DRYOPTERIS FILIX-MAS ROOT; ECHINOCOCCUS GRANULOSUS; ENTEROBIUS VERMICULARIS; GRAPHITE; MERCURIC CHLORIDE; SPIGELIA ANTHELMIA; TAENIA SAGINATA; TAENIA SOLIUM; TANACETUM VULGARE TOP; TEUCRIUM MARUM; TURPENTINE
- Active strength
- 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57520-0061-1 | 57520006101 | 60 mL in 1 BOTTLE, DROPPER (57520-0061-1) | 60 ml | 2010-02-05 | 2022-11-23 | No | No | Current |