Nerve Pro
- Product NDC
- 44911-0495
- 11-digit product format
- 449110495
- Labeler code
- 44911
- Product ID
- 44911-0495_c98c29e3-90b3-4b1d-8a1d-83f9a70075c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Plantago Major, Xanthoxylum Fraxineum, Colocynthis, Magnesia Phosphorica, Agaricus Muscarius, Hypericum Perforatum, Argentum Nitricum, Carboneum Sulphuratum, Curare, Thallium Metallicum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2019-05-14
- Substance
- AMANITA MUSCARIA FRUITING BODY; CARBON DISULFIDE; CITRULLUS COLOCYNTHIS FRUIT PULP; HYPERICUM PERFORATUM WHOLE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PLANTAGO MAJOR WHOLE; SILVER NITRATE; THALLIUM; TUBOCURARINE CHLORIDE; ZANTHOXYLUM AMERICANUM BARK
- Active strength
- 12; 30; 12; 12; 12; 6; 30; 30; 30; 6 [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
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| DIF093I037 | AMANITA MUSCARIA FRUITING BODY | | AMANITA MUSCARIA FRUITING BODY |
| S54S8B99E8 | CARBON DISULFIDE | 75-15-0 | CARBON DISULFIDE |
| 23H32AOH17 | CITRULLUS COLOCYNTHIS FRUIT PULP | | CITRULLUS COLOCYNTHIS FRUIT PULP |
| HF539G9L3Q | MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE | 7782-75-4 | MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE |
| 95IT3W8JZE | SILVER NITRATE | 7761-88-8 | SILVER NITRATE |
| AD84R52XLF | THALLIUM | 7440-28-0 | THALLIUM |
| 900961Z8VR | TUBOCURARINE CHLORIDE | 6989-98-6 | TUBOCURARINE CHLORIDE |
| A4KL1HMZ7T | ZANTHOXYLUM AMERICANUM BARK | | ZANTHOXYLUM AMERICANUM BARK |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 44911-0495-1 | 44911049501 | 30 mL in 1 BOTTLE, DROPPER (44911-0495-1) | 30 ml | 2019-05-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| DRUG FACTS: | Energique, Inc. | Apotheca Company | 2024-10-29 | HUMAN OTC DRUG LABEL | 3 |