| 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 |