| Product NDC: | 49483-356 |
| Proprietary Name: | TIME-GESIC |
| Non Proprietary Name: | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 325; 12.5 mg/1; mg/1 & nbsp; ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49483-356 |
| Labeler Name: | Time-Cap Labs, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121218 |
| Package NDC: | 49483-356-09 |
| Package Description: | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (49483-356-09) |
| NDC Code | 49483-356-09 |
| Proprietary Name | TIME-GESIC |
| Package Description | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (49483-356-09) |
| Product NDC | 49483-356 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121218 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Time-Cap Labs, Inc |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 325; 12.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |