- Product NDC
- 63972-006
- 11-digit product format
- 639720006
- Labeler code
- 63972
- Product ID
- 63972-006_c55f94c7-947d-4001-bc8f-f0bbd17f55ea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACTH, Calcarea carbonica, Magnesia sulphurica, Kali phosphoricum, Nitricum acidum, Benzoicum acidum, Silicea, Arsenicum album, Mercuris solubilis, Phosphorus, Carbo vegetabilis, Nux vomica, Aluminum metallicum, Phytolacca decandra, Baptisia tinctoria, Argentum nitricum, Spigelia anthelmia, Apis mellifica
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- 21st Century Homeopathics, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1975-01-01
- Marketing end
- 0000-00-00
- Substance
- BAPTISIA TINCTORIA ROOT; PHYTOLACCA AMERICANA ROOT; SPIGELIA ANTHELMIA; CORTICOTROPIN; ALUMINUM; APIS MELLIFERA; SILVER NITRATE; ARSENIC TRIOXIDE; BENZOIC ACID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ACTIVATED CHARCOAL; POTASSIUM PHOSPHATE, DIBASIC; MAGNESIUM SULFATE HEPTAHYDRATE; MERCURIUS SOLUBILIS; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; SILICON DIOXIDE
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record