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Alka-Seltzer Plus - 0280-1186-20 - (Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, and Doxylamine succinate)

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Drug Information of Alka-Seltzer Plus

Product NDC: 0280-1186
Proprietary Name: Alka-Seltzer Plus
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, and Doxylamine succinate
Active Ingredient(s):    & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, and Doxylamine succinate
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Alka-Seltzer Plus

Product NDC: 0280-1186
Labeler Name: Bayer HealthCare LLC, Consumer Care
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120703

Package Information of Alka-Seltzer Plus

Package NDC: 0280-1186-20
Package Description: 1 KIT in 1 CARTON * 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Alka-Seltzer Plus

NDC Code 0280-1186-20
Proprietary Name Alka-Seltzer Plus
Package Description 1 KIT in 1 CARTON * 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 0280-1186
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, and Doxylamine succinate
Dosage Form Name KIT
Route Name
Start Marketing Date 20120703
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Bayer HealthCare LLC, Consumer Care
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Alka-Seltzer Plus


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