- Product NDC
- 43742-0240
- 11-digit product format
- 437420240
- Labeler code
- 43742
- Product ID
- 43742-0240_413dc156-30d3-4b80-8371-707f36edbdc4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Chondrus crispus, Fucus vesiculosus, Thyroidinum (suis), Cadmium iodatum, Iodium, Strontium carbonicum, X-Ray,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-12-13
- Marketing end
- 0000-00-00
- Substance
- CHONDRUS CRISPUS; FUCUS VESICULOSUS; THYROID, PORCINE; CADMIUM IODIDE; IODINE; STRONTIUM CARBONATE; ALCOHOL, X-RAY EXPOSED (1000 RAD); RADIUM BROMIDE
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record