Product NDC: | 53799-352 |
Proprietary Name: | Dry Eye Relief |
Non Proprietary Name: | Atropa Belladonna and Euphrasia Stricta and Mercuric Chloride |
Active Ingredient(s): | 6; 6; 6 [hp_X]/.45mL; [hp_X]/.45mL; [hp_X]/.45mL & nbsp; Atropa Belladonna and Euphrasia Stricta and Mercuric Chloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53799-352 |
Labeler Name: | Similasan AG |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19850101 |
Package NDC: | 53799-352-01 |
Package Description: | 270 VIAL, SINGLE-USE in 1 CARTON (53799-352-01) > .45 mL in 1 VIAL, SINGLE-USE |
NDC Code | 53799-352-01 |
Proprietary Name | Dry Eye Relief |
Package Description | 270 VIAL, SINGLE-USE in 1 CARTON (53799-352-01) > .45 mL in 1 VIAL, SINGLE-USE |
Product NDC | 53799-352 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Atropa Belladonna and Euphrasia Stricta and Mercuric Chloride |
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]/.45mL; [hp_X]/.45mL; [hp_X]/.45mL |
Pharmaceutical Classes |