FDA.reportPublic FDA data

RITE AID Regular Strength

Manufacturer
RITE AID CORPORATION
Effective date
2024-10-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:32:12

Label at a glance#

ProductRITE AID 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: potassium 15 mg, sodium 11 mg salicylate 260 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:potassium 15 mg, sodium 11 mg
  • salicylate 260 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

NDC 11822-7060-8

Regular Strength

Pink Bismuth

Bismuth Subsalicylate

Upset Stomach Reliever/Antidiarrheal

original flavor

Relieves:

  • Heartburn
  • Indigestion
  • Nausea
  • Upset Stomach
  • Diarrhea

8 FL. OZ. (236 mL)

*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 SuspensionPSN3
308762bismuth subsalicylate 17.5 MG/ML Oral SuspensionSCD3
308762bismuth subsalicylate 1.75 % Oral SuspensionSY3
308762bismuth subsalicylate 262 MG per 15 ML Oral SuspensionSY3
308762bismuth subsalicylate 524 MG per 30 ML Oral SuspensionSY3
308762bismuth subsalicylate 525 MG per 30 ML Oral SuspensionSY3

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
11822-7060-3RITE AID Regular StrengthPink Bismuth473 mL in 1 BOTTLESUSPENSION4733
11822-7060-3RITE AID Regular StrengthPink Bismuth2 in 1 CARTONSUSPENSION23
11822-7060-6RITE AID Regular StrengthPink Bismuth473 mL in 1 BOTTLESUSPENSION4733
11822-7060-8RITE AID Regular StrengthPink Bismuth236 mL in 1 BOTTLESUSPENSION2363

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-7060RITE AID REGULAR STRENGTH PINK BISMUTH (BISMUTH SUBSALICYLATE) SUSPENSION [RITE AID CORPORATION]3Current NDC, 4 package rows20241101_48fe12a5-5ff0-4d35-8708-675de32a9ed0.zip

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
11822-706011822-7060-8, 11822-7060-6, 11822-7060-3

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

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
RITE AID Regular Strength Pink BismuthBISMUTH SUBSALICYLATERITE AID CORPORATION48fe12a5-5ff0-4d35-8708-675de32a9ed02024-10-31WarningsExact identifier
ndc (package): 11822-7060-6
ndc (package): 11822-7060-8
ndc (package): 11822-7060-3
ndc (product): 11822-7060
ndc11 (package): 11822706006
ndc11 (package): 11822706003
ndc11 (package): 11822706008
spl id: 25befc52-4d82-3d82-e063-6294a90a048c
spl set id: 48fe12a5-5ff0-4d35-8708-675de32a9ed0

Reported adverse events (FAERS/openFDA)#

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