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NightTime Sinus Relief - 59995-007-00 - (ACETAMINOPHEN, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL)

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Drug Information of NightTime Sinus Relief

Product NDC: 59995-007
Proprietary Name: NightTime Sinus Relief
Non Proprietary Name: ACETAMINOPHEN, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL
Active Ingredient(s): 325; 6.25; 5    mg/1; mg/1; mg/1 & nbsp;   ACETAMINOPHEN, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of NightTime Sinus Relief

Product NDC: 59995-007
Labeler Name: Robinson Pharma, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130612

Package Information of NightTime Sinus Relief

Package NDC: 59995-007-00
Package Description: 2 BLISTER PACK in 1 BOX (59995-007-00) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of NightTime Sinus Relief

NDC Code 59995-007-00
Proprietary Name NightTime Sinus Relief
Package Description 2 BLISTER PACK in 1 BOX (59995-007-00) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 59995-007
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOPHEN, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20130612
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Robinson Pharma, Inc.
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 NightTime Sinus Relief


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