Product NDC: | 51621-036 |
Proprietary Name: | ACTIFIRM RECOVERY EYE |
Non Proprietary Name: | ALLANTOIN |
Active Ingredient(s): | .1 mL/20mL & nbsp; ALLANTOIN |
Administration Route(s): | CUTANEOUS |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51621-036 |
Labeler Name: | GOWOONSESANG COSMETICS CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100601 |
Package NDC: | 51621-036-01 |
Package Description: | 20 mL in 1 CARTON (51621-036-01) |
NDC Code | 51621-036-01 |
Proprietary Name | ACTIFIRM RECOVERY EYE |
Package Description | 20 mL in 1 CARTON (51621-036-01) |
Product NDC | 51621-036 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALLANTOIN |
Dosage Form Name | CREAM |
Route Name | CUTANEOUS |
Start Marketing Date | 20100601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | GOWOONSESANG COSMETICS CO., LTD. |
Substance Name | ALLANTOIN |
Strength Number | .1 |
Strength Unit | mL/20mL |
Pharmaceutical Classes |