Product NDC: | 50114-0110 |
Proprietary Name: | Solidago Compositum |
Non Proprietary 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 |
Active Ingredient(s): | 8; 8; 28; 4; 4; 10; 6; 6; 6; 6; 4; 13; 8; 6; 8; 6; 6; 10; 3; 10; 10; 10; 8; 6 [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 & nbsp; 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 |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50114-0110 |
Labeler Name: | Heel Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19930131 |
Package NDC: | 50114-0110-6 |
Package Description: | 10 VIAL in 1 CARTON (50114-0110-6) > 2.2 mL in 1 VIAL |
NDC Code | 50114-0110-6 |
Proprietary Name | Solidago Compositum |
Package Description | 10 VIAL in 1 CARTON (50114-0110-6) > 2.2 mL in 1 VIAL |
Product NDC | 50114-0110 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary 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 Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19930131 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc |
Substance Name | AGATHOSMA BETULINA LEAF; APIS MELLIFERA VENOM; ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; CALCIUM SULFIDE; CAPSICUM; CHONDRODENDRON TOMENTOSUM ROOT; CLERODENDRANTHUS SPICATUS LEAF; CUPRIC SULFATE; EQUISETUM HYEMALE; ESCHERICHIA COLI; HUMAN COXSACKIEVIRUS A; LYTTA VESICATORIA; MERCURIC CHLORIDE; SILVER NITRATE; SMILAX REGELII ROOT; SODIUM PYRUVATE; SOLIDAGO VIRGAUREA FLOWERING TOP; SUS SCROFA RENAL PELVIS; SUS SCROFA URETER; SUS SCROFA URETHRA; SUS SCROFA URINARY BLAD |
Strength Number | 8; 8; 28; 4; 4; 10; 6; 6; 6; 6; 4; 13; 8; 6; 8; 6; 6; 10; 3; 10; 10; 10; 8; 6 |
Strength Unit | [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 |
Pharmaceutical Classes |