TOPCARE ULTRA STRENGTH STOMACH RELIEF- bismuth subsalicylate liquid

Topcare Ultra Strength Stomach Relief by

Drug Labeling and Warnings

Topcare Ultra Strength Stomach Relief by is a Otc medication manufactured, distributed, or labeled by Topco Associates, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT(in each 15 mL)

Bismuth subsalicylate 525 mg

PURPOSE

Upset stomach reliever and anti-diarrheal

USE(S)

relieves:

• diarrhea
• heartburn
• indigestion
• nausea
• upset stomach associated with these symptoms

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
• bloody or black stool
• a bleeding problem

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 may occur

STOP USE AND ASK DOCTOR IF

• symptoms get worse
• 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 immediately.

DIRECTIONS

• shake well before use
• mL = milliliter
• TBSP = tablespoon
• adults and children 12 years and over: 1 dose (1 TBSP or 15 mL) every 1/2 hour as needed
• do not exceed 8 doses (120 mL) in 24 hours
• use until diarrhea stops but not more than 2 days
• children under 12 years: ask a doctor
• drink plenty of fluids to help prevent dehydration caused by diarrhea

OTHER INFORMATION

• each 15 mL or 1 TBSP contains:
• potassium 15 mg
• salicylate 236 mg
• sodium 5 mg
• protect from freezing
• avoid excessive heat (over 104oF or 40oC)
• dosage cup provided

INACTIVE INGREDIENTS

benzoic acid, D&C red # 22, D&C red # 28, flavor, hydroxyethyl cellulose, potassium hydroxide, purified water, saccharin sodium, salicylic acid, simethicone, xanthan gum

PRINCIPAL DISPLAY PANEL

NDC: 76162-022-04
COMPARE TO PEPTO-BISMOL® ULTRA STRENGTH ACTIVE INGREDIENT*
TopCare
ULTRA STRENGTH
Stomach Relief
BISMUTH SUBSALICYLATE 525 mg per 15 mL
UPSET STOMACH RELIEVER/ANTIDIARRHEAL

5 SYMPTOM DIGESTIVE RELIEF

• Heartburn
• Indigestion
• Nausea
• Upset stomach
• Diarrhea

8 FL OZ (236 mL)

NDC: 76162-022-05
COMPARE TO PEPTO-BISMOL® ULTRA STRENGTH ACTIVE INGREDIENT*
TopCare
ULTRA STRENGTH
Stomach Relief
BISMUTH SUBSALICYLATE 525 mg per 15 mL
UPSET STOMACH RELIEVER/ANTIDIARRHEAL

5 SYMPTOM DIGESTIVE RELIEF

• Heartburn
• Indigestion
• Nausea
• Upset stomach
• Diarrhea

12 FL OZ (354 mL)

INGREDIENTS AND APPEARANCE

TOPCARE ULTRA STRENGTH STOMACH RELIEF 
bismuth subsalicylate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76162-022
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ)	BISMUTH SUBSALICYLATE	525 mg  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
BENZOIC ACID (UNII: 8SKN0B0MIM)
D&C RED NO. 22 (UNII: 1678RKX8RT)
D&C RED NO. 28 (UNII: 767IP0Y5NH)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
WATER (UNII: 059QF0KO0R)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SALICYLIC ACID (UNII: O414PZ4LPZ)
HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%) (UNII: L605B5892V)
DIMETHICONE (UNII: 92RU3N3Y1O)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	PINK	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76162-022-05	354 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/05/2022
2	NDC: 76162-022-04	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/05/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M008	01/05/2022

Labeler - Topco Associates, LLC (006935977)