Product NDC: | 37808-666 |
Proprietary Name: | rx act cough and sore throat |
Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate |
Active Ingredient(s): | 500; 15; 6.25 mg/15mL; mg/15mL; mg/15mL & nbsp; Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37808-666 |
Labeler Name: | H E B |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20060704 |
Package NDC: | 37808-666-34 |
Package Description: | 237 mL in 1 BOTTLE (37808-666-34) |
NDC Code | 37808-666-34 |
Proprietary Name | rx act cough and sore throat |
Package Description | 237 mL in 1 BOTTLE (37808-666-34) |
Product NDC | 37808-666 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20060704 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | H E B |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 500; 15; 6.25 |
Strength Unit | mg/15mL; mg/15mL; mg/15mL |
Pharmaceutical Classes |