Virotox WN
- Product NDC
- 57520-0529
- 11-digit product format
- 575200529
- Labeler code
- 57520
- Product ID
- 57520-0529_e18af3ed-4834-4232-8f3f-1c07e66ed643
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea angustifolia, Hydrastis canadensis, Lomatium, Myrrha, Nasturtium aquaticum, Tabebuia impetiginosa, Glandula suprarenalis, Thymus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Apotheca Company
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2010-12-07
- Marketing end
- 2022-09-29
- Substance
- ATROPA BELLADONNA; ECHINACEA ANGUSTIFOLIA; GELSEMIUM SEMPERVIRENS ROOT; GOLDENSEAL; LOMATIUM DISSECTUM ROOT; LYCOPODIUM CLAVATUM SPORE; MYRRH; NASTURTIUM OFFICINALE; RANCID BEEF; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYMUS; TABEBUIA IMPETIGINOSA BARK; WEST NILE VIRUS
- Active strength
- 12 [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], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [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 |
|---|
| 57520-0529-1 | 57520052901 | 30 mL in 1 BOTTLE, DROPPER (57520-0529-1) | 30 ml | 2010-12-07 | 2022-09-29 | No | No | Current |