UP AND UP ANTI DIARRHEAL ANTI GAS- loperamide hydrochloride, simethicone tablet 
Target Corporation

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Target Corporation anti-diarrheal/anti-gas Drug Facts

Active ingredients (in each caplet)

Loperamide HCl 2 mg

Simethicone 125 mg

Purposes

Anti-diarrheal

Anti-gas

Uses

relieves symptoms of diarrhea plus bloating, pressure and cramps, commonly referred to as gas

Warnings

Allergy alert: Do not use if you have ever had a rash or other allergic reaction to loperamide HCl

Heart alert: Taking more than directed can cause serious heart problems or death

Do not use

if you have bloody or black stool
if you have difficulty swallowing

Ask a doctor before use if you have

fever
mucus in the stool
a history of liver disease
a history of abnormal heart rhythm

Ask a doctor or pharmacist before use if you are

taking a prescription drug. Loperamide may interact with certain prescription drugs.

When using this product

tiredness, drowsiness or dizziness may occur. Be careful when driving or operating machinery.

Stop use and ask a doctor if

symptoms get worse
diarrhea lasts for more than 2 days
you get abdominal swelling or bulging. These may be signs of a serious condition.
you have difficulty swallowing the caplet

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 right away. (1-800-222-1222)

Directions

drink plenty of clear fluids to help prevent dehydration caused by diarrhea
take only on an empty stomach (1 hour before or 2 hours after a meal)
take with a full (8 oz.) glass of water
find right dose on chart below. If possible, use weight to dose; otherwise, use age.

adults and children

12 years and over

2 caplets after the first loose stool; 1 caplet after each subsequent loose stool; but no more than 4 caplets in 24 hours

children 9-11 years

(60-95 lbs)

1 caplet after the first loose stool; ½ caplet after each subsequent loose stool; but no more than 3 caplets in 24 hours

children 6-8 years

(48-59 lbs)

1 caplet after the first loose stool; ½ caplet after each subsequent loose stool; but no more than 2 caplets in 24 hours

children 2-5 years

(34 to 47 lbs)

ask a doctor

children under 2 years

(up to 33 lbs)

do not use

Other information

each caplet contains: calcium 165 mg, sodium 3 mg
store between 20°-25°C (68°-77°F). Protect from light.
do not use if printed blister unit is broken o

Inactive ingredients

acesulfame potassium, croscarmellose sodium, dibasic calcium phosphate, maltodextrin, microcrystalline cellulose, natural and artificial flavor, propylene glycol, stearic acid

Questions?

Call 1-888-547-7400

Package/Label Principal Display Panel

Compare to active ingredients in Imodium® Multi-Symptom Relief

loperamide hydrochloride and simethicone tablets, 2 mg/125 mg

anti-diarrheal/anti-gas

multi-symptom relief caplet

relieves symptoms of diarrhea plus:

cramps and pressure, bloating, gas

ACTUAL SIZE

24 CAPLETS*

24 CAPLETS*

(*CAPSULE-SHAPED TABLETS)

anti-diarrheal anti-gas image 1
anti-diarrheal anti-gas image 2
UP AND UP ANTI DIARRHEAL ANTI GAS 
loperamide hydrochloride, simethicone tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-646
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LOPERAMIDE HYDROCHLORIDE (UNII: 77TI35393C) (LOPERAMIDE - UNII:6X9OC3H4II) LOPERAMIDE HYDROCHLORIDE2 mg
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE125 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
ColorWHITEScore2 pieces
ShapeOVALSize17mm
FlavorImprint Code L0R1;2;125
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-646-8918 in 1 CARTON03/14/2019
11 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:11673-646-6224 in 1 CARTON01/06/2021
21 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20983703/14/2019
Labeler - Target Corporation (006961700)

Revised: 1/2021
Document Id: 162f774a-dcd5-4138-ad34-2eac58a32998
Set id: ef75085c-95df-4901-9c97-069fcfc3eef7
Version: 4
Effective Time: 20210106
 
Target Corporation