| Product NDC: | 68210-0102 |
| Proprietary Name: | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and DOXYLAMINE SUCCINATE |
| Non Proprietary Name: | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and DOXYLAMINE SUCCINATE |
| Active Ingredient(s): | 325; 15; 6.25 mg/1; mg/1; mg/1 & nbsp; ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and DOXYLAMINE SUCCINATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68210-0102 |
| Labeler Name: | SPIRIT PHARMACEUTICALS, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091015 |
| Package NDC: | 68210-0102-6 |
| Package Description: | 2500 CAPSULE, LIQUID FILLED in 1 BOX (68210-0102-6) |
| NDC Code | 68210-0102-6 |
| Proprietary Name | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and DOXYLAMINE SUCCINATE |
| Package Description | 2500 CAPSULE, LIQUID FILLED in 1 BOX (68210-0102-6) |
| Product NDC | 68210-0102 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and DOXYLAMINE SUCCINATE |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20091015 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SPIRIT PHARMACEUTICALS, LLC |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 325; 15; 6.25 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |