| Product NDC: | 58852-000 |
| Proprietary Name: | Mens ComBack HAIR REGROWTH TREATMENT EXTRA STRENGTH UNSCENTED |
| Non Proprietary Name: | MINOXIDIL |
| Active Ingredient(s): | 50 mg/mL & nbsp; MINOXIDIL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58852-000 |
| Labeler Name: | Combback International LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076239 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130606 |
| Package NDC: | 58852-000-02 |
| Package Description: | 1 BOTTLE in 1 CARTON (58852-000-02) > 60 mL in 1 BOTTLE |
| NDC Code | 58852-000-02 |
| Proprietary Name | Mens ComBack HAIR REGROWTH TREATMENT EXTRA STRENGTH UNSCENTED |
| Package Description | 1 BOTTLE in 1 CARTON (58852-000-02) > 60 mL in 1 BOTTLE |
| Product NDC | 58852-000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MINOXIDIL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130606 |
| Marketing Category Name | ANDA |
| Labeler Name | Combback International LLC |
| Substance Name | MINOXIDIL |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |