alka-seltzer plus cough, mucus and congestion day and night powermax

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 cough, mucus and congestion day and night powermax
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 0280-0035
Product ID 0280-0035_4523aa8a-0db4-5337-e063-6394a90a8bda
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 02800035
Hyphenated Format 0280-0035

Supplemental Identifiers

RxCUI
1297288 1656815 2634364
UPC
0016500584223

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 cough, mucus and congestion day and night powermax (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 (0280-0035-01) * 3 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 3 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (1)

0280-0035-01 1 KIT in 1 CARTON (0280-0035-01) * 3 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 3 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

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

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4523aa8a-0db4-5337-e063-6394a90a8bda", "openfda": {"upc": ["0016500584223"], "rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["a68df74d-dd26-3ae9-e053-2995a90a08d6"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0280-0035-01)  *  3 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  3 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-0035-01", "marketing_start_date": "20200601"}], "brand_name": "Alka-Seltzer Plus Cough, Mucus and Congestion Day and Night Powermax", "product_id": "0280-0035_4523aa8a-0db4-5337-e063-6394a90a8bda", "dosage_form": "KIT", "product_ndc": "0280-0035", "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 Cough, Mucus and Congestion Day and Night Powermax", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}