UP AND UP 5-SYMPTOM DIGESTIVE RELIEF- bismuth subsalicylate tablet

up and up 5-symptom digestive relief by

Drug Labeling and Warnings

up and up 5-symptom digestive relief by is a Otc medication manufactured, distributed, or labeled by Target Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each caplet)

Bismuth subsalicylate 262 mg

Purpose

Upset stomach reliever and anti-diarrheal

Uses

relieves

• ▪ heartburn
• ▪ indigestion
• ▪ nausea
• ▪ upset stomach
• ▪ diarrhea

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 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 may occur.

Stop use and ask a doctor if

• ▪ symptoms get worse or last more than 2 days
• ▪ ringing in the ears occurs 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 immediately.1-800-222-1222.

Directions

• ▪ swallow with water, do not chew
• ▪ adults and children 12 years and older: 2 caplets every 1/2 to 1 hour as needed
• ▪ do not exceed 8 doses (16 caplets) 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

• ▪ each caplet contains: calcium 27 mg
• ▪ sodium 3 mg
• ▪ salicylate 99 mg
• ▪ low sodium
• ▪ sugar free
• ▪ avoid excessive heat (over 104°F or 40°C)

Inactive ingredients

calcium carbonate, crospovidone, D&C red#27 aluminum lake, magnesium stearate, microcrystalline cellulose, sodium lauryl sulfate.

PRINCIPAL DISPLAY PANEL -

NDC: 11673-125-20

Compare to active ingredient in Pepto-Bismol® Caplets*

5- symptom digestive relief

relief of upset stomach, nausea, heartburn, indigestion, diarrhea

40 CAPLETS

*This product is not manufactured or distributed by Procter & Gamble Inc. the distributor of PEPTO-BISMOL®

TAMPER EVIDENT DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING.

245 05 0375 R01 ID285492

Dist.by Target Corp., Mpls ., MN 55403

©2015 Target Brands, Inc.

Shop Target.com

Guest Services 1-800-910-6874

INGREDIENTS AND APPEARANCE

UP AND UP 5-SYMPTOM DIGESTIVE RELIEF 
bismuth subsalicylate tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-125
Route of Administration	ORAL

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

Inactive Ingredients
Ingredient Name	Strength
calcium carbonate (UNII: H0G9379FGK)
CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)
D&C RED NO. 27 (UNII: 2LRS185U6K)
magnesium stearate (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)

Product Characteristics
Color	PINK (mottled light pink)	Score	no score
Shape	OVAL (Oblong Caplet)	Size	16mm
Flavor		Imprint Code	RP125
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-125-20	40 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/07/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part335	09/07/2015

Labeler - Target Corporation (006961700)