United States · FDA National Drug Code directory

Ultra Strength digestive 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
0363-1302_447d20f5-798d-ca2a-e063-6294a90ada0d
Product NDC
0363-1302
Form
TABLET
Composition / generic term
Bismuth subsalicylate
Labeler
WALGREENS CO.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20220926
Source listing expiry
20261231

Source-listed ingredients

  • BISMUTH SUBSALICYLATE — 525 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (0363-1302-02) / 24 TABLET in 1 BOTTLE · 0363-1302-02

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 →