| 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 |