Alka-Seltzer Plus Severe Cold PowerFast Fizz Day and Night

SPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBayer HealthCare LLC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0280006901
1 KIT in 1 CARTON (0280-0069-01) * 1 TABLET, EFFERVESCENT in 1 POUCH * 1 TABLET, EFFERVESCENT in 1 POUCH

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "ORAL",
  "spl_meta": {
    "4a16b6e5-f0c6-e3a4-e063-6294a90a85ad": {
      "match": "brand_token",
      "title": "ALKA-SELTZER EXTRA STRENGTH PAIN RELIEF (ANHYDROUS CITRIC ACID, ASPIRIN) TABLET, EFFERVESCENT [BAYER HEALTHCARE LLC.]",
      "spl_version": "1",
      "published_date": "2026-02-09"
    }
  },
  "productid": "0280-0069_45264ea9-aed7-8b75-e063-6394a90a74c1",
  "productndc": "0280-0069",
  "dosage_form": "KIT",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": null,
  "proprietary_name": "Alka-Seltzer Plus Severe Cold PowerFast Fizz Day and Night",
  "active_ingred_unit": null,
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate",
  "start_marketing_date": "20210805",
  "active_numerator_strength": null
}

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