- Product NDC
- 44911-0722
- 11-digit product format
- 449110722
- Labeler code
- 44911
- Product ID
- 44911-0722_b7249b51-5056-4cd4-8912-6f51923118e6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Baryta Carbonica, Calcarea Carbonica, Calcarea Iodata, Fucus Vesiculosus, Iodium, Lapis Albus, Levothyroxinum, Natrum Muriaticum, Pulsatilla (Vulgaris), Selenium Metallicum, Spongia Tosta, Thyroidinum (Suis)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-09-30
- Substance
- BARIUM CARBONATE; CALCIUM HEXAFLUOROSILICATE; CALCIUM IODIDE; FUCUS VESICULOSUS; IODINE; LEVOTHYROXINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PULSATILLA VULGARIS WHOLE; SELENIUM; SODIUM CHLORIDE; SPONGIA OFFICINALIS SKELETON, ROASTED; THYROID
- Active strength
- 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [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; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Thyroxine [CS], l-Thyroxine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes