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Strumeel Forte Rx Oral Drops
Strumeel Forte Rx Oral Drops - 50114-1144-4 - (SPONGIA OFFICINALIS SKELETON, ROASTED and CALCIUM IODIDE and FUCUS VESICULOSUS and SILICON DIOXIDE and)
Drug Information of Strumeel Forte Rx Oral Drops
| Product NDC: | 50114-1144 |
| Proprietary Name: | Strumeel Forte Rx Oral Drops |
| Non Proprietary Name: | SPONGIA OFFICINALIS SKELETON, ROASTED and CALCIUM IODIDE and FUCUS VESICULOSUS and SILICON DIOXIDE and |
| Active Ingredient(s): | 3; 3; 8; 2 [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL & nbsp; SPONGIA OFFICINALIS SKELETON, ROASTED and CALCIUM IODIDE and FUCUS VESICULOSUS and SILICON DIOXIDE and |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Strumeel Forte Rx Oral Drops
| Product NDC: | 50114-1144 |
| Labeler Name: | Heel Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19860131 |
Package Information of Strumeel Forte Rx Oral Drops
| Package NDC: | 50114-1144-4 |
| Package Description: | 50 mL in 1 BOTTLE (50114-1144-4) |
NDC Information of Strumeel Forte Rx Oral Drops
| NDC Code | 50114-1144-4 |
| Proprietary Name | Strumeel Forte Rx Oral Drops |
| Package Description | 50 mL in 1 BOTTLE (50114-1144-4) |
| Product NDC | 50114-1144 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SPONGIA OFFICINALIS SKELETON, ROASTED and CALCIUM IODIDE and FUCUS VESICULOSUS and SILICON DIOXIDE and |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19860131 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc |
| Substance Name | CALCIUM IODIDE; FUCUS VESICULOSUS; SILICON DIOXIDE; SPONGIA OFFICINALIS SKELETON, ROASTED |
| Strength Number | 3; 3; 8; 2 |
| Strength Unit | [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL |
| Pharmaceutical Classes |
