Product NDC: | 55312-926 |
Proprietary Name: | Day Relief Night Relief Free |
Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl |
Active Ingredient(s): | & nbsp; Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55312-926 |
Labeler Name: | Western Family Foods Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20070817 |
Package NDC: | 55312-926-01 |
Package Description: | 1 KIT in 1 PACKAGE (55312-926-01) * 296 mL in 1 BOTTLE (55312-041-38) * 296 mL in 1 BOTTLE (55312-656-38) |
NDC Code | 55312-926-01 |
Proprietary Name | Day Relief Night Relief Free |
Package Description | 1 KIT in 1 PACKAGE (55312-926-01) * 296 mL in 1 BOTTLE (55312-041-38) * 296 mL in 1 BOTTLE (55312-656-38) |
Product NDC | 55312-926 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20070817 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Western Family Foods Inc |
Substance Name | |
Strength Number | |
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