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Day Time Sinus - 55315-099-16 - (Acetaminophen and Phenylephrine Hydrochloride)

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Drug Information of Day Time Sinus

Product NDC: 55315-099
Proprietary Name: Day Time Sinus
Non Proprietary Name: Acetaminophen and Phenylephrine Hydrochloride
Active Ingredient(s): 325; 5    mg/1; mg/1 & nbsp;   Acetaminophen and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Day Time Sinus

Product NDC: 55315-099
Labeler Name: Freds Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120815

Package Information of Day Time Sinus

Package NDC: 55315-099-16
Package Description: 2 BLISTER PACK in 1 CARTON (55315-099-16) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Day Time Sinus

NDC Code 55315-099-16
Proprietary Name Day Time Sinus
Package Description 2 BLISTER PACK in 1 CARTON (55315-099-16) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 55315-099
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Phenylephrine Hydrochloride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120815
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Freds Inc
Substance Name ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Day Time Sinus


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