| Product NDC: | 53799-345 |
| Proprietary Name: | Dry Eye Relief |
| Non Proprietary Name: | Belladonna, Euphrasia, Mercurius sublimatus |
| Active Ingredient(s): | 6; 6; 6 [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL & nbsp; Belladonna, Euphrasia, Mercurius sublimatus |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 53799-345 |
| Labeler Name: | Similasan AG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19850101 |
| Package NDC: | 53799-345-11 |
| Package Description: | 10 mL in 1 BOTTLE, DROPPER (53799-345-11) |
| NDC Code | 53799-345-11 |
| Proprietary Name | Dry Eye Relief |
| Package Description | 10 mL in 1 BOTTLE, DROPPER (53799-345-11) |
| Product NDC | 53799-345 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Belladonna, Euphrasia, Mercurius sublimatus |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19850101 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Similasan AG |
| Substance Name | ATROPA BELLADONNA; EUPHRASIA STRICTA; MERCURIC CHLORIDE |
| Strength Number | 6; 6; 6 |
| Strength Unit | [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL |
| Pharmaceutical Classes |