- Product NDC
- 43406-0071
- 11-digit product format
- 434060071
- Labeler code
- 43406
- Product ID
- 43406-0071_d3b754f0-5a03-44e6-bbc9-0ace31b246ce
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- American Ginseng, Black Cohosh, Spigelia Anthelmia, Silver Nitrate, Arsenic Trioxide, Gold, Strychnos Ignatti Seed, Lachesis Muta Venom, Lycopodium Clavatum Spore, Sodium Chloride, Phosphoric Acid, Platinum, Pulsatilla Vulgaris, Sepia Officinalis Juice, Thuja Occidentalis Leafy Twig,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Natural Creations, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2007-05-29
- Marketing end
- 0000-00-00
- Substance
- AMERICAN GINSENG; BLACK COHOSH; SPIGELIA ANTHELMIA; SILVER NITRATE; ARSENIC TRIOXIDE; GOLD; STRYCHNOS IGNATII SEED; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; SODIUM CHLORIDE; PHOSPHORIC ACID; PLATINUM; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; THUJA OCCIDENTALIS LEAFY TWIG
- 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; [hp_X]/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record