| Product NDC: | 63029-202 | 
| Proprietary Name: | BC Arthritis | 
| Non Proprietary Name: | Aspirin and Caffeine | 
| Active Ingredient(s): | 1000; 65 mg/1; mg/1 & nbsp; Aspirin and Caffeine | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | POWDER | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 63029-202 | 
| Labeler Name: | Medtech Products Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part343 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20120601 | 
| Package NDC: | 63029-202-02 | 
| Package Description: | 24 POWDER in 1 BOX (63029-202-02) | 
| NDC Code | 63029-202-02 | 
| Proprietary Name | BC Arthritis | 
| Package Description | 24 POWDER in 1 BOX (63029-202-02) | 
| Product NDC | 63029-202 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Aspirin and Caffeine | 
| Dosage Form Name | POWDER | 
| Route Name | ORAL | 
| Start Marketing Date | 20120601 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | Medtech Products Inc. | 
| Substance Name | ASPIRIN; CAFFEINE | 
| Strength Number | 1000; 65 | 
| Strength Unit | mg/1; mg/1 | 
| Pharmaceutical Classes |