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 |