alka-seltzer plus maximum strength day and night cold and flu

Generic: dextromethorphan hydrobromide, acetaminophen, phenylephrine hydrochloride, doxylamine succinate

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 and night cold and flu
Generic Name dextromethorphan hydrobromide, acetaminophen, phenylephrine hydrochloride, doxylamine succinate
Labeler bayer healthcare llc.
Dosage Form KIT
Routes
ORAL
Manufacturer
Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 0280-0040
Product ID 0280-0040_452615d3-7d63-4fa6-e063-6394a90a5dfd
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2020-10-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02800040
Hyphenated Format 0280-0040

Supplemental Identifiers

RxCUI
1086997 1297288 2634363
UPC
0016500555315

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 and night cold and flu (source: ndc)
Generic Name dextromethorphan hydrobromide, acetaminophen, phenylephrine hydrochloride, doxylamine succinate (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 5 mg
  • 6.25 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (0280-0040-01) * 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (1)

0280-0040-01 1 KIT in 1 CARTON (0280-0040-01) * 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "452615d3-7d63-4fa6-e063-6394a90a5dfd", "openfda": {"upc": ["0016500555315"], "rxcui": ["1086997", "1297288", "2634363"], "spl_set_id": ["b13d5132-cb91-3cf6-e053-2a95a90aa47c"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0280-0040-01)  *  12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-0040-01", "marketing_start_date": "20201026"}], "brand_name": "Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu", "product_id": "0280-0040_452615d3-7d63-4fa6-e063-6394a90a5dfd", "dosage_form": "KIT", "product_ndc": "0280-0040", "generic_name": "dextromethorphan hydrobromide, acetaminophen, phenylephrine hydrochloride, doxylamine succinate", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201026", "listing_expiration_date": "20261231"}