- Product NDC
- 50114-5324
- 11-digit product format
- 501145324
- Labeler code
- 50114
- Product ID
- 50114-5324_6bd1d376-97d2-4876-96e6-31c7ad4903cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SULFUR, THUJA OCCIDENTALIS LEAFY TWIG, VACCINIA VIRUS STRAIN NEW YORK CITY BOARD, GONORRHEAL URETHRAL SECRETION HUMAN,SODIUM CHLORIDE, NERIUM OLEANDER LEAF,CICUTA VIROSA ROOT,
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Heel Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1993-01-31
- Marketing end
- 0000-00-00
- Substance
- SULFUR; THUJA OCCIDENTALIS LEAFY TWIG; VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN; BUFO BUFO CUTANEOUS GLAND; SCABIES LESION LYSATE (HUMAN); GONORRHEAL URETHRAL SECRETION HUMAN; NERIUM OLEANDER LEAF; CICUTA VIROSA ROOT; POTASSIUM DICHROMATE
- Active strength
- 6 [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL
- Pharmacologic classes
- Live Vaccinia Virus Vaccine [EPC],Actively Acquired Immunity [PE],Smallpox Vaccine [CS],Vaccines, Live, Unattenuated [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record