- Product NDC
- 70163-0043
- 11-digit product format
- 701630043
- Labeler code
- 70163
- Product ID
- 70163-0043_0b1dae4a-5af6-4f34-804b-8a50f61b8c5a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Chamomilla, Graphites, Kali Carbonicum, Kali Oxalicum, Kali Phosphoricum, Magnesia Phosphorica, Natrum Muriaticum, Natrum Phosphoricum, Natrum Sulphuricum, Nux Vomica, Rheum (Palmatum), Robinia Pseudoacacia
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- NaturalCare
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2026-03-25
- Substance
- DIBASIC POTASSIUM PHOSPHATE; GRAPHITE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MATRICARIA CHAMOMILLA WHOLE; POTASSIUM CARBONATE; POTASSIUM OXALATE; RHEUM PALMATUM ROOT; ROBINIA PSEUDOACACIA BARK; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED
- Active strength
- 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 30 [hp_X]/1; [hp_C]/1; [hp_X]/1; [hp_X]/1; [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
- Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Plant Proteins [CS], Potassium Compounds [CS], Potassium Salt [EPC], Seed Storage Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes