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DayTime Nitetime Sinus Relief - 36800-102-48 - (Acetaminophen, Doxylamine succinate, Phenylephrine HCl)

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Drug Information of DayTime Nitetime Sinus Relief

Product NDC: 36800-102
Proprietary Name: DayTime Nitetime Sinus Relief
Non Proprietary Name: Acetaminophen, Doxylamine succinate, Phenylephrine HCl
Active Ingredient(s):    & nbsp;   Acetaminophen, Doxylamine succinate, Phenylephrine HCl
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of DayTime Nitetime Sinus Relief

Product NDC: 36800-102
Labeler Name: TOP CARE (Topco Associates LLC)
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130115

Package Information of DayTime Nitetime Sinus Relief

Package NDC: 36800-102-48
Package Description: 1 KIT in 1 CARTON (36800-102-48) * 8 CAPSULE in 1 BLISTER PACK * 8 CAPSULE in 1 BLISTER PACK

NDC Information of DayTime Nitetime Sinus Relief

NDC Code 36800-102-48
Proprietary Name DayTime Nitetime Sinus Relief
Package Description 1 KIT in 1 CARTON (36800-102-48) * 8 CAPSULE in 1 BLISTER PACK * 8 CAPSULE in 1 BLISTER PACK
Product NDC 36800-102
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Doxylamine succinate, Phenylephrine HCl
Dosage Form Name KIT
Route Name
Start Marketing Date 20130115
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name TOP CARE (Topco Associates LLC)
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of DayTime Nitetime Sinus Relief


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