United States · FDA National Drug Code directory
Dual Action Pain Relief
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 11673-924_22ecfa46-dbe4-249f-e063-6394a90a70af
- Product NDC
- 11673-924
- Form
- TABLET
- Composition / generic term
- Acetaminophen, Ibuprofen
- Labeler
- TARGET CORPORATION
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230711
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 125 mg/1
- ACETAMINOPHEN — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (11673-924-75) / 72 TABLET in 1 BOTTLE · 11673-924-75
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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