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