alka-seltzer plus maximum strength cough, mucus and congestion powermax
Generic: acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
Labeler: bayer healthcare llc.Drug Facts
Product Profile
Brand Name
alka-seltzer plus maximum strength cough, mucus and congestion powermax
Generic Name
acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
Labeler
bayer healthcare llc.
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, guaifenesin 200 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0280-0061
Product ID
0280-0061_45262b77-58b2-6e5f-e063-6394a90a443c
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2020-06-01
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02800061
Hyphenated Format
0280-0061
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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 cough, mucus and congestion powermax (source: ndc)
Generic Name
acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 10 mg/1
- 200 mg/1
- 5 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (0280-0061-01) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
- 2 BLISTER PACK in 1 CARTON (0280-0061-02) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Packages (2)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45262b77-58b2-6e5f-e063-6394a90a443c", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0016500584209"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1656815"], "spl_set_id": ["a6a2dd4a-a3c8-2dfa-e053-2995a90ada86"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0280-0061-01) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-0061-01", "marketing_start_date": "20200601"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0280-0061-02) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-0061-02", "marketing_start_date": "20200601"}], "brand_name": "Alka-Seltzer Plus Maximum Strength Cough, Mucus and Congestion Powermax", "product_id": "0280-0061_45262b77-58b2-6e5f-e063-6394a90a443c", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "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": "0280-0061", "generic_name": "acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Maximum Strength Cough, Mucus and Congestion Powermax", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}