| 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 |