Home NDC 56062-372-16 Stomach Relief
Product NDC 56062-372
Requested package NDC 56062-372-16
11-digit product format 560620372
Labeler code 56062
Product ID 56062-372_953a91ab-e732-4240-9410-b6c8a679fc42
Type HUMAN OTC DRUG
Nonproprietary name Bismuth subsalicylate
Dosage form LIQUID
Route ORAL
Labeler Publix Supermarkets, Inc.
Application part335
Marketing category OTC MONOGRAPH FINAL
Marketing start 2014-12-31
Marketing end 0000-00-00
Substance BISMUTH SUBSALICYLATE
Active strength 525 mg/30mL
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 11 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded BISMUTH SUBSALICYLATE ACTIVE INGREDIENT 62TEY51RR1 STOMACH RELIEF ORIGINAL FORMULA (BISMUTH SUBSALICYLATE) LIQUID [PUBLIX SUPERMARKETS, INC.] 1 SALICYLIC ACID ACTIVE MOIETY O414PZ4LPZ STOMACH RELIEF ORIGINAL FORMULA (BISMUTH SUBSALICYLATE) LIQUID [PUBLIX SUPERMARKETS, INC.] 1 BENZOIC ACID INACTIVE INGREDIENT 8SKN0B0MIM STOMACH RELIEF ORIGINAL FORMULA (BISMUTH SUBSALICYLATE) LIQUID [PUBLIX SUPERMARKETS, INC.] 1 D&C RED NO. 22 INACTIVE INGREDIENT 1678RKX8RT STOMACH RELIEF ORIGINAL FORMULA (BISMUTH SUBSALICYLATE) LIQUID [PUBLIX SUPERMARKETS, INC.] 1 D&C RED NO. 28 INACTIVE INGREDIENT 767IP0Y5NH STOMACH RELIEF ORIGINAL FORMULA (BISMUTH SUBSALICYLATE) LIQUID [PUBLIX SUPERMARKETS, INC.] 1 MAGNESIUM ALUMINUM SILICATE INACTIVE INGREDIENT 6M3P64V0NC STOMACH RELIEF ORIGINAL FORMULA (BISMUTH SUBSALICYLATE) LIQUID [PUBLIX SUPERMARKETS, INC.] 1 METHYLCELLULOSE (1500 MPA.S) INACTIVE INGREDIENT P0NTE48364 STOMACH RELIEF ORIGINAL FORMULA (BISMUTH SUBSALICYLATE) LIQUID [PUBLIX SUPERMARKETS, INC.] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY STOMACH RELIEF ORIGINAL FORMULA (BISMUTH SUBSALICYLATE) LIQUID [PUBLIX SUPERMARKETS, INC.] 1 SALICYLIC ACID INACTIVE INGREDIENT O414PZ4LPZ STOMACH RELIEF ORIGINAL FORMULA (BISMUTH SUBSALICYLATE) LIQUID [PUBLIX SUPERMARKETS, INC.] 1 SODIUM SALICYLATE INACTIVE INGREDIENT WIQ1H85SYP STOMACH RELIEF ORIGINAL FORMULA (BISMUTH SUBSALICYLATE) LIQUID [PUBLIX SUPERMARKETS, INC.] 1 SORBIC ACID INACTIVE INGREDIENT X045WJ989B STOMACH RELIEF ORIGINAL FORMULA (BISMUTH SUBSALICYLATE) LIQUID [PUBLIX SUPERMARKETS, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R STOMACH RELIEF ORIGINAL FORMULA (BISMUTH SUBSALICYLATE) LIQUID [PUBLIX SUPERMARKETS, INC.] 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 56062-372-16 56062037216 473 mL in 1 BOTTLE, PLASTIC (56062-372-16) 473 ml 2014-12-31 0000-00-00 No No Current