United States · FDA National Drug Code directory

dg health dual back pain reliever

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
55910-508_83981f7c-bbb0-4912-b7ca-3f4a2418ffca
Product NDC
55910-508
Form
TABLET, FILM COATED
Composition / generic term
acetaminophen, ibuprofen
Labeler
Dolgencorp Inc
Marketing category
ANDA
Marketing start / end (source format)
20240426
Source listing expiry
20261231

Source-listed ingredients

  • ACETAMINOPHEN — 250 mg/1
  • IBUPROFEN — 125 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (55910-508-23) / 72 TABLET, FILM COATED in 1 BOTTLE · 55910-508-23
  • 1 BOTTLE in 1 CARTON (55910-508-68) / 36 TABLET, FILM COATED in 1 BOTTLE · 55910-508-68

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →