Leg Cramp Relief
- Product NDC
- 43689-0004
- 11-digit product format
- 436890004
- Labeler code
- 43689
- Product ID
- 43689-0004_95b9ea3b-a321-4199-a5ba-bf66a41dd24c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Causticum, Colocynthis, Cuprum Metallicum, Magnesia Phosphorica, Phytolacca Decandra, Rhus Tox, Stannum Metallicum, Veratrum Album
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- The Magni Company
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-10-10
- Marketing end
- 2023-12-17
- Substance
- CAUSTICUM; CITRULLUS COLOCYNTHIS FRUIT PULP; COPPER; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PHYTOLACCA AMERICANA ROOT; TIN; TOXICODENDRON PUBESCENS LEAF; VERATRUM ALBUM ROOT
- Active strength
- 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- Pharmacologic classes
- Calculi Dissolution Agent [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Large Intestinal Motility [PE], Inhibit Ovum Fertilization [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 |
|---|
| 43689-0004-1 | 43689000401 | 125 TABLET in 1 BOTTLE (43689-0004-1) | 125 tablet | 2012-10-10 | 2023-12-17 | No | No | Current |