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Stye Eye Relief
Stye Eye Relief - 53799-350-11 - (Conium maculatum and Graphites and Sulphur)
Drug Information of Stye Eye Relief
| Product NDC: | 53799-350 |
| Proprietary Name: | Stye Eye Relief |
| Non Proprietary Name: | Conium maculatum and Graphites and Sulphur |
| Active Ingredient(s): | 6; 12; 12 [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL & nbsp; Conium maculatum and Graphites and Sulphur |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Stye Eye Relief
| Product NDC: | 53799-350 |
| Labeler Name: | Similasan AG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20050102 |
Package Information of Stye Eye Relief
| Package NDC: | 53799-350-11 |
| Package Description: | 10 mL in 1 BOTTLE, DROPPER (53799-350-11) |
NDC Information of Stye Eye Relief
| NDC Code | 53799-350-11 |
| Proprietary Name | Stye Eye Relief |
| Package Description | 10 mL in 1 BOTTLE, DROPPER (53799-350-11) |
| Product NDC | 53799-350 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Conium maculatum and Graphites and Sulphur |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20050102 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Similasan AG |
| Substance Name | CONIUM MACULATUM FLOWERING TOP; GRAPHITE; SULFUR |
| Strength Number | 6; 12; 12 |
| Strength Unit | [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL |
| Pharmaceutical Classes |
