VASCULAR
- Product NDC
- 44911-0140
- 11-digit product format
- 449110140
- Labeler code
- 44911
- Product ID
- 44911-0140_596fec71-3296-4ab4-8022-9880583cbb6a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aesculus Hippocastanum, Collinsonia Canadensis, Echinacea (Angustifolia), Hamamelis Virginiana, Pulsatilla (Vulgaris), Arnica Montana, Carbo Vegetabilis, Graphites, Hydrofluoricum Acidum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Paeonia Officinalis, Sepia
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-01-30
- Marketing end
- 2022-09-13
- Substance
- HORSE CHESTNUT; COLLINSONIA CANADENSIS ROOT; ECHINACEA ANGUSTIFOLIA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; PULSATILLA VULGARIS; ARNICA MONTANA; ACTIVATED CHARCOAL; GRAPHITE; HYDROFLUORIC ACID; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; PAEONIA OFFICINALIS ROOT; SEPIA OFFICINALIS JUICE
- Active strength
- 3 [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
- 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 |
|---|
| 44911-0140-1 | 44911014001 | 30 mL in 1 BOTTLE, DROPPER (44911-0140-1) | 30 ml | 2015-01-30 | 2022-09-13 | No | No | Current |