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 |