| Product NDC: | 50289-3250 |
| Proprietary Name: | AER |
| Non Proprietary Name: | Witch Hazel |
| Active Ingredient(s): | .5 mL/mL & nbsp; Witch Hazel |
| Administration Route(s): | RECTAL; TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50289-3250 |
| Labeler Name: | Birchwood Laboratories Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111230 |
| Package NDC: | 50289-3250-1 |
| Package Description: | 40 APPLICATOR in 1 JAR (50289-3250-1) > 2.8 mL in 1 APPLICATOR |
| NDC Code | 50289-3250-1 |
| Proprietary Name | AER |
| Package Description | 40 APPLICATOR in 1 JAR (50289-3250-1) > 2.8 mL in 1 APPLICATOR |
| Product NDC | 50289-3250 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Witch Hazel |
| Dosage Form Name | SOLUTION |
| Route Name | RECTAL; TOPICAL |
| Start Marketing Date | 20111230 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Birchwood Laboratories Inc |
| Substance Name | WITCH HAZEL |
| Strength Number | .5 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |