- Product NDC
- 50114-0110
- 11-digit product format
- 501140110
- Labeler code
- 50114
- Product ID
- 50114-0110_cdc6114c-1b6f-4329-a612-fdc1535b6c06
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SOLIDAGO VIRGAUREA FLOWERING TOP and BAPTISIA TINCTORIA ROOT and BERBERIS VULGARIS ROOT BARK and EQUISETUM HYEMALE and SILVER NITRATE and LYTTA VESICATORIA and CAPSICUM and CUPRIC SULFATE and CLERODENDRANTHUS SPICATUS LEAF and CHONDRODENDRON TOMENTOSUM ROOT and SMILAX REGELII ROOT and TURPENTINE OIL and APIS MELLIFERA VENOM and AGATHOSMA BETULINA LEAF and HUMAN COXSACKIEVIRUS A and MERCURIC CHLORIDE and SUS SCROFA URINARY BLADDER and CALCIUM SULFIDE and SODIUM PYRUVATE
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Heel Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1993-01-31
- Marketing end
- 0000-00-00
- Substance
- SOLIDAGO VIRGAUREA FLOWERING TOP; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; EQUISETUM HYEMALE; SILVER NITRATE; LYTTA VESICATORIA; CAPSICUM; CUPRIC SULFATE; CLERODENDRANTHUS SPICATUS LEAF; CHONDRODENDRON TOMENTOSUM ROOT; SMILAX REGELII ROOT; TURPENTINE OIL; APIS MELLIFERA VENOM; AGATHOSMA BETULINA LEAF; HUMAN COXSACKIEVIRUS A; MERCURIC CHLORIDE; SUS SCROFA URINARY BLADDER; CALCIUM SULFIDE; SODIUM PYRUVATE; SUS SCROFA RENAL PELVIS; SUS SCROFA URETER; SUS SCROFA URETHRA; ESCHERICHIA COLI; ARSENIC TRIOXIDE
- Active strength
- 3 [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record