Product NDC: | 54868-4698 |
Proprietary Name: | Sodium Chloride |
Non Proprietary Name: | Sodium Chloride |
Active Ingredient(s): | 50 mg/g & nbsp; Sodium Chloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-4698 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20060330 |
Package NDC: | 54868-4698-0 |
Package Description: | 1 TUBE in 1 CARTON (54868-4698-0) > 3.5 g in 1 TUBE |
NDC Code | 54868-4698-0 |
Proprietary Name | Sodium Chloride |
Package Description | 1 TUBE in 1 CARTON (54868-4698-0) > 3.5 g in 1 TUBE |
Product NDC | 54868-4698 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Chloride |
Dosage Form Name | OINTMENT |
Route Name | OPHTHALMIC |
Start Marketing Date | 20060330 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | SODIUM CHLORIDE |
Strength Number | 50 |
Strength Unit | mg/g |
Pharmaceutical Classes |