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Sinus Nighttime - 41520-101-16 - (Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride)

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Drug Information of Sinus Nighttime

Product NDC: 41520-101
Proprietary Name: Sinus Nighttime
Non Proprietary Name: Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride
Active Ingredient(s): 325; 6.25; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Sinus Nighttime

Product NDC: 41520-101
Labeler Name: American Sales Company (Care One)
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121031

Package Information of Sinus Nighttime

Package NDC: 41520-101-16
Package Description: 2 BLISTER PACK in 1 CARTON (41520-101-16) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Sinus Nighttime

NDC Code 41520-101-16
Proprietary Name Sinus Nighttime
Package Description 2 BLISTER PACK in 1 CARTON (41520-101-16) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 41520-101
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20121031
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name American Sales Company (Care One)
Substance Name ACETAMINOPHEN; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 6.25; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Sinus Nighttime


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