Product NDC: | 0813-0799 |
Proprietary Name: | Fem pH |
Non Proprietary Name: | Acetic Acid and Oxyquinoline sulfate |
Active Ingredient(s): | .009; .00025 g/g; g/g & nbsp; Acetic Acid and Oxyquinoline sulfate |
Administration Route(s): | VAGINAL |
Dosage Form(s): | JELLY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0813-0799 |
Labeler Name: | Pharmics, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19990715 |
Package NDC: | 0813-0799-55 |
Package Description: | 50 g in 1 TUBE (0813-0799-55) |
NDC Code | 0813-0799-55 |
Proprietary Name | Fem pH |
Package Description | 50 g in 1 TUBE (0813-0799-55) |
Product NDC | 0813-0799 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Acetic Acid and Oxyquinoline sulfate |
Dosage Form Name | JELLY |
Route Name | VAGINAL |
Start Marketing Date | 19990715 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Pharmics, Inc. |
Substance Name | ACETIC ACID; OXYQUINOLINE SULFATE |
Strength Number | .009; .00025 |
Strength Unit | g/g; g/g |
Pharmaceutical Classes |