- Product NDC
- 57520-0954
- 11-digit product format
- 575200954
- Labeler code
- 57520
- Product ID
- 57520-0954_7dd4de79-5475-440b-b78e-4514f95e7a27
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Codfish, Flounder, Halibut, Mackerel, Tuna, Clam, Crab, Oyster, Scallops, Shrimp, Belladonna, Carbo animalis, Colocynthis, Kali Carbonicum, Lycopodium clavatum, Pulsatilla,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Apotheca Company
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-11-17
- Marketing end
- 0000-00-00
- Substance
- COD, UNSPECIFIED; EUROPEAN FLOUNDER; ATLANTIC HALIBUT; SCOMBEROMORUS CAVALLA WHOLE; TUNA, UNSPECIFIED; QUAHOG, UNSPECIFIED; SHRIMP, UNSPECIFIED; BLUE CRAB; EDIBLE OYSTER; SEA SCALLOP; ATROPA BELLADONNA; CARBO ANIMALIS; CITRULLUS COLOCYNTHIS FRUIT PULP; POTASSIUM CARBONATE; LYCOPODIUM CLAVATUM SPORE; PULSATILLA VULGARIS
- Active strength
- 9 [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; [hp_X]/mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record