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Daytime Sinus - 63941-341-51 - (Acetaminophen and Phenylephrine HCI)

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Drug Information of Daytime Sinus

Product NDC: 63941-341
Proprietary Name: Daytime Sinus
Non Proprietary Name: Acetaminophen and Phenylephrine HCI
Active Ingredient(s): 325; 5    mg/1; mg/1 & nbsp;   Acetaminophen and Phenylephrine HCI
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Daytime Sinus

Product NDC: 63941-341
Labeler Name: VALU MERCHANDISERS COMPANY
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120529

Package Information of Daytime Sinus

Package NDC: 63941-341-51
Package Description: 2 BLISTER PACK in 1 BOX (63941-341-51) > 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Daytime Sinus

NDC Code 63941-341-51
Proprietary Name Daytime Sinus
Package Description 2 BLISTER PACK in 1 BOX (63941-341-51) > 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 63941-341
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Phenylephrine HCI
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120529
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name VALU MERCHANDISERS COMPANY
Substance Name ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Daytime Sinus


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