Product NDC: | 53346-1359 |
Proprietary Name: | DR. RECKEWEG R59 Vesiculine |
Non Proprietary Name: | Calcarea carbonica 12X, Fucus vesiculosus 4X, Graphites 12X, Natrum sulphuricum 4X, Spongia tosta 4X |
Active Ingredient(s): | 4; 12; 12; 4; 4 [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL & nbsp; Calcarea carbonica 12X, Fucus vesiculosus 4X, Graphites 12X, Natrum sulphuricum 4X, Spongia tosta 4X |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53346-1359 |
Labeler Name: | PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19860601 |
Package NDC: | 53346-1359-5 |
Package Description: | 50 mL in 1 BOTTLE (53346-1359-5) |
NDC Code | 53346-1359-5 |
Proprietary Name | DR. RECKEWEG R59 Vesiculine |
Package Description | 50 mL in 1 BOTTLE (53346-1359-5) |
Product NDC | 53346-1359 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Calcarea carbonica 12X, Fucus vesiculosus 4X, Graphites 12X, Natrum sulphuricum 4X, Spongia tosta 4X |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19860601 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO |
Substance Name | FUCUS VESICULOSUS; GRAPHITE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SODIUM SULFATE; SPONGIA OFFICINALIS SKELETON, ROASTED |
Strength Number | 4; 12; 12; 4; 4 |
Strength Unit | [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL |
Pharmaceutical Classes |