- Product NDC
- 43742-0009
- 11-digit product format
- 437420009
- Labeler code
- 43742
- Product ID
- 43742-0009_e8baa3af-451c-4041-a7b5-418f40e0f880
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alfalfa, Laminaria digitata, Symphytum officinale, Calcarea carbonica, Ferrum metallicum, Agate, Iodium, Magnesium metallicum, Manganum metallicum, Quartz, Tarentula cubensis, Cuprum metallicum, Phosphorus, X-ray, Carbon dioxide, Silicea Magnetis polus articus, Magnetis polus australis,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-04-19
- Marketing end
- 2021-10-25
- Substance
- ALFALFA; LAMINARIA DIGITATA; COMFREY ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; IRON; SILICON DIOXIDE; IODINE; MAGNESIUM; MANGANESE; CITHARACANTHUS SPINICRUS; COPPER; PHOSPHORUS; ALCOHOL, X-RAY EXPOSED (1000 RAD); CARBON DIOXIDE
- 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; [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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record