alka-seltzer plus maximum strength day cold and flu powermax gels

Generic: acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride

Labeler: bayer healthcare llc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name alka-seltzer plus maximum strength day cold and flu powermax gels
Generic Name acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride
Labeler bayer healthcare llc.
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, phenylephrine hydrochloride 5 mg/1

Manufacturer
Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 0280-1630
Product ID 0280-1630_45267e98-74cd-6121-e063-6294a90a5166
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2018-07-02

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] sigma-1 agonist [epc] sigma-1 receptor agonists [moa] uncompetitive n-methyl-d-aspartate receptor antagonist [epc] uncompetitive nmda receptor antagonists [moa] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02801630
Hyphenated Format 0280-1630

Supplemental Identifiers

RxCUI
1086997
UPC
0016500576808
UNII
362O9ITL9D 9D2RTI9KYH 04JA59TNSJ

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name alka-seltzer plus maximum strength day cold and flu powermax gels (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 10 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (0280-1630-16) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (0280-1630-24) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (2)

Ingredients (3)

acetaminophen (325 mg/1) dextromethorphan hydrobromide (10 mg/1) phenylephrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45267e98-74cd-6121-e063-6294a90a5166", "openfda": {"upc": ["0016500576808"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["6f2d18f6-935f-9215-e053-2a91aa0aedd3"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0280-1630-16)  / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-1630-16", "marketing_start_date": "20180702"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0280-1630-24)  / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-1630-24", "marketing_start_date": "20180702"}], "brand_name": "Alka-Seltzer Plus Maximum Strength Day Cold and Flu PowerMax Gels", "product_id": "0280-1630_45267e98-74cd-6121-e063-6294a90a5166", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0280-1630", "generic_name": "acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Maximum Strength Day Cold and Flu PowerMax Gels", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180702", "listing_expiration_date": "20261231"}