alka-seltzer pain relief

Generic: alka-seltzer pain relief

Labeler: bayer healthcare llc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name alka-seltzer pain relief
Generic Name alka-seltzer pain relief
Labeler bayer healthcare llc.
Dosage Form TABLET, EFFERVESCENT
Routes
ORAL
Active Ingredients

aspirin 325 mg/1

Manufacturer
Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 0280-8251
Product ID 0280-8251_4975f0ff-047f-7fca-e063-6294a90aef2f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2027-12-31
Marketing Start 2025-12-01

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc] platelet aggregation inhibitor [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]
Physiologic Effect
decreased prostaglandin production [pe] decreased platelet aggregation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02808251
Hyphenated Format 0280-8251

Supplemental Identifiers

RxCUI
2606079
UPC
0016500603610
UNII
R16CO5Y76E
NUI
N0000000160 N0000008836 M0001335 N0000175722 N0000175578 N0000008832

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 pain relief (source: ndc)
Generic Name alka-seltzer pain relief (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
source: ndc
Packaging
  • 12 POUCH in 1 CARTON (0280-8251-24) / 2 TABLET, EFFERVESCENT in 1 POUCH
  • 18 POUCH in 1 CARTON (0280-8251-36) / 2 TABLET, EFFERVESCENT in 1 POUCH
  • 36 POUCH in 1 CARTON (0280-8251-72) / 2 TABLET, EFFERVESCENT in 1 POUCH
source: ndc

Packages (3)

Ingredients (1)

aspirin (325 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4975f0ff-047f-7fca-e063-6294a90aef2f", "openfda": {"nui": ["N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832"], "upc": ["0016500603610"], "unii": ["R16CO5Y76E"], "rxcui": ["2606079"], "spl_set_id": ["4975f0ff-0480-7fca-e063-6294a90aef2f"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_pe": ["Decreased Prostaglandin Production [PE]", "Decreased Platelet Aggregation [PE]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CARTON (0280-8251-24)  / 2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "0280-8251-24", "marketing_start_date": "20251201"}, {"sample": false, "description": "18 POUCH in 1 CARTON (0280-8251-36)  / 2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "0280-8251-36", "marketing_start_date": "20251201"}, {"sample": false, "description": "36 POUCH in 1 CARTON (0280-8251-72)  / 2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "0280-8251-72", "marketing_start_date": "20251201"}], "brand_name": "Alka-Seltzer Pain Relief", "product_id": "0280-8251_4975f0ff-047f-7fca-e063-6294a90aef2f", "dosage_form": "TABLET, EFFERVESCENT", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]"], "product_ndc": "0280-8251", "generic_name": "Alka-Seltzer Pain Relief", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Pain Relief", "active_ingredients": [{"name": "ASPIRIN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251201", "listing_expiration_date": "20271231"}