Product NDC: | 60681-1822 |
Proprietary Name: | Pleo Muc |
Non Proprietary Name: | mucor racemosus |
Active Ingredient(s): | 5 [hp_X]/mL & nbsp; mucor racemosus |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60681-1822 |
Labeler Name: | Sanum Kehlbeck GmbH & Co KG |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20110615 |
Package NDC: | 60681-1822-1 |
Package Description: | 2 POUCH in 1 CARTON (60681-1822-1) > 5 AMPULE in 1 POUCH > .5 mL in 1 AMPULE |
NDC Code | 60681-1822-1 |
Proprietary Name | Pleo Muc |
Package Description | 2 POUCH in 1 CARTON (60681-1822-1) > 5 AMPULE in 1 POUCH > .5 mL in 1 AMPULE |
Product NDC | 60681-1822 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | mucor racemosus |
Dosage Form Name | LIQUID |
Route Name | OPHTHALMIC |
Start Marketing Date | 20110615 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Sanum Kehlbeck GmbH & Co KG |
Substance Name | MUCOR RACEMOSUS |
Strength Number | 5 |
Strength Unit | [hp_X]/mL |
Pharmaceutical Classes |