| Product NDC: | 52904-470 |
| Proprietary Name: | Allertness Aid |
| Non Proprietary Name: | Caffeine |
| Active Ingredient(s): | 200 mg/1 & nbsp; Caffeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52904-470 |
| Labeler Name: | Select Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part340 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121015 |
| Package NDC: | 52904-470-02 |
| Package Description: | 2 TABLET in 1 PACKET (52904-470-02) |
| NDC Code | 52904-470-02 |
| Proprietary Name | Allertness Aid |
| Package Description | 2 TABLET in 1 PACKET (52904-470-02) |
| Product NDC | 52904-470 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Caffeine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121015 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Select Corporation |
| Substance Name | CAFFEINE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |