Product NDC: | 55618-1001 |
Proprietary Name: | Jilgyungyi |
Non Proprietary Name: | ALLANTOIN |
Active Ingredient(s): | .2 1/1 & nbsp; ALLANTOIN |
Administration Route(s): | VAGINAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55618-1001 |
Labeler Name: | HA U DONG CHUN |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20130611 |
Package NDC: | 55618-1001-1 |
Package Description: | 20 TABLET in 1 PACKAGE (55618-1001-1) |
NDC Code | 55618-1001-1 |
Proprietary Name | Jilgyungyi |
Package Description | 20 TABLET in 1 PACKAGE (55618-1001-1) |
Product NDC | 55618-1001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALLANTOIN |
Dosage Form Name | TABLET |
Route Name | VAGINAL |
Start Marketing Date | 20130611 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | HA U DONG CHUN |
Substance Name | ALLANTOIN |
Strength Number | .2 |
Strength Unit | 1/1 |
Pharmaceutical Classes |