| Product NDC: | 68169-0061 |
| Proprietary Name: | FIRST AID RESEARCH ZINC OXYDE PLUS |
| Non Proprietary Name: | MENTHOL AND ZINC OXIDE |
| Active Ingredient(s): | .44; 20 g/100g; g/100g & nbsp; MENTHOL AND ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68169-0061 |
| Labeler Name: | TAI GUK PHARM. CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100928 |
| Package NDC: | 68169-0061-1 |
| Package Description: | 1 TUBE in 1 CARTON (68169-0061-1) > 57 g in 1 TUBE |
| NDC Code | 68169-0061-1 |
| Proprietary Name | FIRST AID RESEARCH ZINC OXYDE PLUS |
| Package Description | 1 TUBE in 1 CARTON (68169-0061-1) > 57 g in 1 TUBE |
| Product NDC | 68169-0061 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL AND ZINC OXIDE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100928 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | TAI GUK PHARM. CO., LTD. |
| Substance Name | MENTHOL; ZINC OXIDE |
| Strength Number | .44; 20 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |