FDA.reportPublic FDA data

PUBLIX Regular Strength

Manufacturer
PUBLIX SUPER MARKETS, INC
Effective date
2025-10-28
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:41:01

Label at a glance#

ProductPUBLIX Regular Strength Pink Bismuth
Active ingredientBISMUTH SUBSALICYLATE
Label structure9 sections

Indications and uses

relieves travelers’ diarrhea diarrhea upset stomach due to overindulgence in food and drink, including: heartburn indigestion nausea gas belching fullness

Dosage and administration

shake well before use only use dose cup provided adults and children 12 years and over: 30 mL 1 (dose) every 1/2 hour or 60 mL (2 doses) every hour as needed for diarrhea/traveler’s diarrhea 30 mL (1 dose) every ½ hour as needed for overindulgence (upset stomach, heartburn, indigestion, nausea) do not exceed 8 doses (240 mL) in 24 hours use until diarrhea stops but not more than 2 days children under 12 years: ask...

Storage and handling

each 30 mL contains: sodium 10 mg salicylate 261 mg low sodium sugar free store at room temperature protect from freezing avoid excessive heat (over 104°F or 40°C)

Label contents#

Full prescribing information#

Active ingredient (in each 30 mL dose)

OTC - ACTIVE INGREDIENT SECTION

Bismuth subsalicylate 525 mg

Purposes

OTC - PURPOSE SECTION

Upset stomach reliever and antidiarrheal

Uses

INDICATIONS & USAGE SECTION

relieves

  • travelers’ diarrhea
  • diarrhea
  • upset stomach due to overindulgence in food and drink, including:
  • heartburn
  • indigestion
  • nausea
  • gas
  • belching
  • fullness

Warnings

WARNINGS SECTION

Reye’s syndrome:Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea or vomiting occur, consult a doctor because these symptoms could be an early sign of Reye’s syndrome, a rare but serious illness.

Allergy alert: Contains salicylate.Do not take if you are

  • allergic to salicylates (including aspirin)
  • taking other salicylate products

Do not use if you have

OTC - DO NOT USE SECTION

  • an ulcer
  • a bleeding problem
  • bloody or black stool

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • fever
  • mucus in the stool

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

taking any drug for

  • anticoagulation (thinning the blood)
  • diabetes
  • gout
  • arthritis

When using this product

OTC - WHEN USING SECTION

a temporary, but harmless, darkening of the stool and/or tongue may occur

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • symptoms get worse or last more than 2 days
  • ringing in the ears or loss of hearing occurs
  • diarrhea lasts more than 2 days

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away at (1-800-222-1222).

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake well before use
  • only use dose cup provided
  • adults and children 12 years and over:30 mL 1 (dose) every 1/2 hour or 60 mL (2 doses) every hour as needed for diarrhea/traveler’s diarrhea
  • 30 mL (1 dose) every ½ hour as needed for overindulgence (upset stomach, heartburn, indigestion, nausea)
  • do not exceed 8 doses (240 mL) in 24 hours
  • use until diarrhea stops but not more than 2 days
  • children under 12 years:ask a doctor
  • drink plenty of clear fluids to help prevent dehydration caused by diarrhea

Other information

STORAGE AND HANDLING SECTION

  • each 30 mL contains:sodium 10 mg
  • salicylate 261 mg
  • low sodium
  • sugar free
  • store at room temperature
  • protect from freezing
  • avoid excessive heat (over 104°F or 40°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

carboxymethylcellulose sodium, D&C Red No. 22, D&C Red No. 28, flavor, microcrystalline cellulose, potassium hydroxide, potassium sorbate, purified water, salicylic acid, simethicone emulsion, sodium benzoate, sucralose, xanthan gum

Questions or comments?

OTC - QUESTIONS SECTION

1-866-467-2748

DO NOT USE IF IMPRINTED SHRINK BAND IS MISSING OR BROKEN.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

*C ompare to the active ingredient in Pepto-Bismol® Regular Strength

Regular Strength

Pink Bismuth

Bismuth Subsalicylate 525 mg

Upset Stomach Reliever/Antidiarrheal

original flavor

Relieves:

  • Heartburn
  • Indigestion
  • Nausea
  • Upset Stomach
  • Diarrhea

*This product is not manufactured or distributed by Procter & Gamble, distributor of Pepto-Bismol ®Regular Strength.

Package Label 236 mL

Regular Strength Stomach Relief 236 mL
Regular Strength Stomach Relief 236 mL

Package Label 473 mL

SPL UNCLASSIFIED SECTION

Regular Strength Stomach Relief 473 mL
Regular Strength Stomach Relief 473 mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308762bismuth subsalicylate 525 MG in 30 mL Oral SuspensionPSN5
308762bismuth subsalicylate 17.5 MG/ML Oral SuspensionSCD5
308762bismuth subsalicylate 1.75 % Oral SuspensionSY5
308762bismuth subsalicylate 262 MG per 15 ML Oral SuspensionSY5
308762bismuth subsalicylate 524 MG per 30 ML Oral SuspensionSY5
308762bismuth subsalicylate 525 MG per 30 ML Oral SuspensionSY5

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130041415536739GTIN-13: 0041415536739
EAN-13: 0041415536739
GTIN-12: 041415536739
UPC-A: 041415536739
GTIN storage (14 digits): 00041415536739		70608TOP artwork.png.jpg
BarcodeEAN-130041415537736GTIN-13: 0041415537736
EAN-13: 0041415537736
GTIN-12: 041415537736
UPC-A: 041415537736
GTIN storage (14 digits): 00041415537736		302 88 stomach-relief-image.jpg
QR code linkQR Codewww.publix.com/p/215161?Source=qrcode70608TOP artwork.png.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0be8e4ae-4d57-49f3-b3a9-e4728b4e8d15Product name120240313
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41415-706-08PUBLIX Regular StrengthPink Bismuth236 mL in 1 BOTTLESUSPENSION2365
41415-706-16PUBLIX Regular StrengthPink Bismuth473 mL in 1 BOTTLESUSPENSION4735

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41415-70641415-706-08, 41415-706-16

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIEDK679OBS311IACT
D&C RED NO. 221678RKX8RTIACT
D&C RED NO. 28767IP0Y5NHIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT
SALICYLIC ACIDO414PZ4LPZIACT
DIMETHICONE, UNSPECIFIED92RU3N3Y1OIACT
SODIUM BENZOATEOJ245FE5EUIACT
SUCRALOSE96K6UQ3ZD4IACT
XANTHAN GUMTTV12P4NEEIACT
BISMUTH SUBSALICYLATE62TEY51RR1ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-10-29full-release2026-06-01 00:31:23

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PUBLIX Regular Strength Pink BismuthBISMUTH SUBSALICYLATEPUBLIX SUPER MARKETS, INCa9b2da55-5171-4702-9808-5b937182da022025-10-28WarningsExact identifier
ndc (package): 41415-706-16
ndc (package): 41415-706-08
ndc (product): 41415-706
ndc11 (package): 41415070608
ndc11 (package): 41415070616
spl id: 42375585-2843-fa23-e063-6294a90af057
spl set id: a9b2da55-5171-4702-9808-5b937182da02

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.