Product NDC: | 56062-090 |
Proprietary Name: | daytime pe nitetime |
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: | 56062-090 |
Labeler Name: | Publix Super Markets Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121029 |
Package NDC: | 56062-090-57 |
Package Description: | 1 KIT in 1 CARTON (56062-090-57) * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Code | 56062-090-57 |
Proprietary Name | daytime pe nitetime |
Package Description | 1 KIT in 1 CARTON (56062-090-57) * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
Product NDC | 56062-090 |
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 | 20121029 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Publix Super Markets Inc |
Substance Name | |
Strength Number | |
Strength Unit | |
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