- Product NDC
- 17312-029
- 11-digit product format
- 173120029
- Labeler code
- 17312
- Product ID
- 17312-029_f1ed5fe0-1f49-1fcf-e053-2995a90aa9b1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aloe, Citrullus Colocynthis, Croton Tiglium, Lycopodium Clavatum, Magnesium Sulfate Heptahydrate, Phosphoric Acid, Thuja Occidentalis
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- TRP Company
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-04-15
- Marketing end
- 0000-00-00
- Substance
- ALOE; CITRULLUS COLOCYNTHIS FRUIT PULP; CROTON TIGLIUM SEED; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM SULFATE HEPTAHYDRATE; PHOSPHORIC ACID; THUJA OCCIDENTALIS LEAFY TWIG
- Active strength
- 5 [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], 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
- 2024-12-31
- Current FDA listing
- Historical FDA.report record