PEPTIC RELIEF- bismuth subsalicylate tablet, chewable

Peptic Relief by

Drug Labeling and Warnings

Peptic Relief by is a Otc medication manufactured, distributed, or labeled by L&R Distributors, Inc., LNK International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each tablet)

Bismuth subsalicylate 262 mg 

Purpose

Upset stomach reliever/antidiarrheal 

Uses

relieves:

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

Warnings

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 and 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

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

Ask a doctor before use if you have

• fever
• mucus in the stool 

Ask a doctor or pharmacist before use if you are

taking any drug for

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

When using this product

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

Stop use and ask a doctor if

• 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,

ask a health professional before use. 

Keep out of reach of children.

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

Directions

• chew or dissolve in mouth
• drink plenty of clear fluids to help prevent dehydration caused by diarrhea
• adults and children 12 years and over: 2 tablets every 1/2 to 1 hour as needed. Do not exceed 8 doses (16 tablets) in 24 hours.
• use until diarrhea stops, but not more than 2 days
• children under 12 years: ask a doctor 

Other information

• each tablet contains: calcium 40 mg, salicylate 102 mg
• TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF CELLOPHANE UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING
• see end flap for expiration date and lot number
  
• store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)
• avoid excessive heat
• store in a dry place

Inactive ingredients

calcium carbonate, cherry flavor, D&C red #27 aluminum lake, D&C red #30 aluminum lake, FD&C red #40 aluminum lake, magnesium stearate, mannitol, povidone, saccharin sodium, stearic acid, talc 

Questions or comments?

1-800-426-9391

Principal Display Panel

select brand®
the lower price name brand

NDC: 15127-319-01

Cherry Flavored

Peptic
Relief 

Bismuth subsalicylate 262 mg
Upset Stomach Reliever/Antidiarrheal

Provides relief for:
Upset Stomach Indigestion
Nausea Heartburn Diarrhea

*Compare to the Active Ingredient of Pepto-Bismol®

30 Chewable Tablets

TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF CELLOPHANE UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING

*This product is not manufactured or distributed by Procter & Gamble, owner of the registered trademark Pepto-Bismol®.

50844      ORG021531901

Distributed by:
SELECT BRAND® DISTRIBUTORS
Pine Bluff, AR 71603 USA
AC (870) 535-3635

Select Brand 44-319

INGREDIENTS AND APPEARANCE

PEPTIC RELIEF 
bismuth subsalicylate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 15127-319
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ, BISMUTH CATION - UNII:ZS9CD1I8YE)	BISMUTH SUBSALICYLATE	262 mg

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK)
D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)
D&C RED NO. 30 (UNII: 2S42T2808B)
FD&C RED NO. 40 (UNII: WZB9127XOA)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MANNITOL (UNII: 3OWL53L36A)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
STEARIC ACID (UNII: 4ELV7Z65AP)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	PINK (dark pink)	Score	no score
Shape	ROUND	Size	16mm
Flavor	CHERRY	Imprint Code	44;319
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 15127-319-01	5 in 1 CARTON	07/16/1998	08/03/2021
1		6 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part335	07/16/1998	08/03/2021

Labeler - L&R Distributors, Inc. (012578514)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		038154464	PACK(15127-319)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		832867894	MANUFACTURE(15127-319)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		832867837	PACK(15127-319)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		868734088	PACK(15127-319)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		967626305	PACK(15127-319)