Product NDC: | 54948-100 |
Proprietary Name: | BAEKNYONDONGAN TREATMENT |
Non Proprietary Name: | WITCH HAZEL |
Active Ingredient(s): | .55 mL/550mL & nbsp; WITCH HAZEL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54948-100 |
Labeler Name: | MIX & MATCH CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110803 |
Package NDC: | 54948-100-01 |
Package Description: | 550 mL in 1 BOTTLE (54948-100-01) |
NDC Code | 54948-100-01 |
Proprietary Name | BAEKNYONDONGAN TREATMENT |
Package Description | 550 mL in 1 BOTTLE (54948-100-01) |
Product NDC | 54948-100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | WITCH HAZEL |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20110803 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | MIX & MATCH CO., LTD. |
Substance Name | WITCH HAZEL |
Strength Number | .55 |
Strength Unit | mL/550mL |
Pharmaceutical Classes |