alka-seltzer plus maximum strength cough, mucus and congestion day and night

Generic: acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, 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 cough, mucus and congestion day and night
Generic Name acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride
Labeler bayer healthcare, llc.
Dosage Form KIT
Routes
ORAL
Manufacturer
Bayer HealthCare, LLC.

Identifiers & Regulatory

Product NDC 0280-0062
Product ID 0280-0062_45263262-6498-654f-e063-6394a90a4683
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2020-06-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02800062
Hyphenated Format 0280-0062

Supplemental Identifiers

RxCUI
1297288 1656815 2634364
UPC
0016500584216

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 cough, mucus and congestion day and night (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 200 mg
  • 5 mg
  • 6.25 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (0280-0062-01) * 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (1)

0280-0062-01 1 KIT in 1 CARTON (0280-0062-01) * 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Alka-Seltzer Plus Maximum Strength Cough, Mucus and Congestion Day and Night ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45263262-6498-654f-e063-6394a90a4683", "openfda": {"upc": ["0016500584216"], "rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["a6b8dc25-0fb9-1823-e053-2a95a90adf93"], "manufacturer_name": ["Bayer HealthCare, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0280-0062-01)  *  2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-0062-01", "marketing_start_date": "20200601"}], "brand_name": "Alka-Seltzer Plus Maximum Strength Cough, Mucus and Congestion Day and Night", "product_id": "0280-0062_45263262-6498-654f-e063-6394a90a4683", "dosage_form": "KIT", "product_ndc": "0280-0062", "generic_name": "acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, 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 Day and Night", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}