United States · FDA National Drug Code directory
up and up arthritis 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
- 11673-569_3f9d13e9-6d6c-41cd-b2ba-9567247172eb
- Product NDC
- 11673-569
- Form
- GEL
- Composition / generic term
- diclofenac sodium
- Labeler
- Target Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200819
- Source listing expiry
- 20261231
Source-listed ingredients
- DICLOFENAC SODIUM — 10 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (11673-569-01) / 100 g in 1 TUBE · 11673-569-01
- 1 TUBE in 1 CARTON (11673-569-03) / 150 g in 1 TUBE · 11673-569-03
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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