alka-seltzer plus cold day and night powermax gels

Generic: acetaminophen, dextromethorphan hydrobromide, phenylephrine bitartrate, 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 cold day and night powermax gels
Generic Name acetaminophen, dextromethorphan hydrobromide, phenylephrine bitartrate, doxylamine succinate
Labeler bayer healthcare llc.
Dosage Form KIT
Routes
ORAL
Manufacturer
Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 0280-0099
Product ID 0280-0099_452656ff-79e2-0871-e063-6294a90ac49d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2018-07-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02800099
Hyphenated Format 0280-0099

Supplemental Identifiers

RxCUI
1086997 1297288 2634363
UPC
0016500583462

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 cold day and night powermax gels (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, phenylephrine bitartrate, doxylamine succinate (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 5 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (0280-0099-01) * 2 CAPSULE in 1 BLISTER PACK / 8 CAPSULE, LIQUID FILLED in 1 CAPSULE * 2 CAPSULE in 1 BLISTER PACK / 4 CAPSULE, LIQUID FILLED in 1 CAPSULE
source: ndc

Packages (1)

0280-0099-01 1 KIT in 1 CARTON (0280-0099-01) * 2 CAPSULE in 1 BLISTER PACK / 8 CAPSULE, LIQUID FILLED in 1 CAPSULE * 2 CAPSULE in 1 BLISTER PACK / 4 CAPSULE, LIQUID FILLED in 1 CAPSULE

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Alka-Seltzer Plus Cold Day and Night PowerMax gels ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "452656ff-79e2-0871-e063-6294a90ac49d", "openfda": {"upc": ["0016500583462"], "rxcui": ["1086997", "1297288", "2634363"], "spl_set_id": ["f6c73f61-f4fc-377f-e053-6294a90a3797"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0280-0099-01)  *  2 CAPSULE in 1 BLISTER PACK / 8 CAPSULE, LIQUID FILLED in 1 CAPSULE *  2 CAPSULE in 1 BLISTER PACK / 4 CAPSULE, LIQUID FILLED in 1 CAPSULE", "package_ndc": "0280-0099-01", "marketing_start_date": "20180914"}], "brand_name": "Alka-Seltzer Plus Cold Day and Night PowerMax gels", "product_id": "0280-0099_452656ff-79e2-0871-e063-6294a90ac49d", "dosage_form": "KIT", "product_ndc": "0280-0099", "generic_name": "Acetaminophen, Dextromethorphan hydrobromide, Phenylephrine bitartrate, Doxylamine succinate", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Cold Day and Night PowerMax gels", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180701", "listing_expiration_date": "20261231"}