| 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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