| Product NDC: | 52904-468 |
| Proprietary Name: | Pain Relief Maximum Strength |
| Non Proprietary Name: | Acetaminophen,Aspirin,Caffeine |
| Active Ingredient(s): | 250; 250; 65 mg/1; mg/1; mg/1 & nbsp; Acetaminophen,Aspirin,Caffeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52904-468 |
| Labeler Name: | Select Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121015 |
| Package NDC: | 52904-468-02 |
| Package Description: | 2 TABLET, COATED in 1 PACKET (52904-468-02) |
| NDC Code | 52904-468-02 |
| Proprietary Name | Pain Relief Maximum Strength |
| Package Description | 2 TABLET, COATED in 1 PACKET (52904-468-02) |
| Product NDC | 52904-468 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen,Aspirin,Caffeine |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121015 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Select Corporation |
| Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
| Strength Number | 250; 250; 65 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |