Product NDC: | 68169-0130 |
Proprietary Name: | PREMIER VALUE ZINC OXIDE |
Non Proprietary Name: | ZINC OXIDE |
Active Ingredient(s): | 20 g/100g & nbsp; ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68169-0130 |
Labeler Name: | TAI GUK PHARM. CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101108 |
Package NDC: | 68169-0130-7 |
Package Description: | 1 TUBE in 1 CARTON (68169-0130-7) > 56 g in 1 TUBE |
NDC Code | 68169-0130-7 |
Proprietary Name | PREMIER VALUE ZINC OXIDE |
Package Description | 1 TUBE in 1 CARTON (68169-0130-7) > 56 g in 1 TUBE |
Product NDC | 68169-0130 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ZINC OXIDE |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20101108 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | TAI GUK PHARM. CO., LTD. |
Substance Name | ZINC OXIDE |
Strength Number | 20 |
Strength Unit | g/100g |
Pharmaceutical Classes |