Sciatica
- Product NDC
- 44911-0215
- 11-digit product format
- 449110215
- Labeler code
- 44911
- Product ID
- 44911-0215_dcbd2321-a2d8-433a-88b3-bc12fa9b9e4f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum Napellus, Aesculus Hippocastanum, Colocynthis, Gnaphalium Polycephalum, Hypericum Perforatum, Magnesia Phosphorica, Plumbum Metallicum, Rhus Tox, Arnica Montana
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-07-14
- Marketing end
- 2025-04-30
- Substance
- ACONITUM NAPELLUS; ARNICA MONTANA; CITRULLUS COLOCYNTHIS FRUIT PULP; HORSE CHESTNUT; HYPERICUM PERFORATUM; LEAD; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PSEUDOGNAPHALIUM OBTUSIFOLIUM; TOXICODENDRON PUBESCENS LEAF
- Active strength
- 30 [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- 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 |
|---|
| 44911-0215-1 | 44911021501 | 30 mL in 1 BOTTLE, DROPPER (44911-0215-1) | 30 ml | 2015-07-14 | 2025-04-30 | No | No | Current |