HANDY SOLUTIONS ANTI-DIARRHEAL- loperamide hydrochloride tablet 
Navajo Manufacturing Company Inc.

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Handy Solutions Anti-Diarrheal

Drug Facts

Active ingredient (in each caplet)

Loperamide Hydrochloride 2 mg

Purpose

Antidiarrheal

Uses

Controls the symptoms of diarrhea, including Traveler’s diarrhea

Warnings

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

Do not use

• if you have bloody or black stools

Ask a doctor before use if you have

• a fever
• mucus in stool
• a history of liver disease

Ask a doctor or pharmacist before use if you are

• taking antibiotics

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 more than 2 days
• you get abdominal swelling or bulging. These may be signs of a serious condition.

If you are pregnant or breast feeding,

ask a health professional before use.

Keep this and all drugs out of the reach of children.

In case of accidental overdose, contact a physician or Poison Control Center right away.

Directions

do not use more than directed
drink plenty of clear fluids to help prevent dehydration caused by diarrhea

 Adults and children (12 years and older): Take 2 caplets after the first
loose bowel movement
followed by 1 caplet after each
subsequent loose bowel
movement but no more than
4 caplets in 24 hours.
 Children under 12 years: Do not give to children under
12 years of age.

Other information

• store between 68º - 77ºF (20º - 25ºC)
• tamper-evident sealed packets
• do not use any opened or torn packet

Inactive ingredients

anhydrous lactose, croscarmellose sodium, crospovidone, D&C yellow # 10, FD&C blue # 1, hydrogenated vegetable oil, magnesium stearate, powdered cellulose, pregelatinized starch

Questions or comments?

1-800-525-5097

Package Labeling:

HS Anti-Diarrheal

HANDY SOLUTIONS ANTI-DIARRHEAL 
loperamide hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67751-162(NDC:47682-200)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LOPERAMIDE HYDROCHLORIDE (UNII: 77TI35393C) (LOPERAMIDE - UNII:6X9OC3H4II) LOPERAMIDE HYDROCHLORIDE2 mg
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
CROSPOVIDONE (UNII: 2S7830E561)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
Product Characteristics
Colorgreen (green) Score2 pieces
ShapeOVAL (OVAL) Size10mm
FlavorImprint Code 123
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67751-162-011 in 1 CARTON09/21/2016
11 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07409109/21/2016
Labeler - Navajo Manufacturing Company Inc. (091917799)
Establishment
NameAddressID/FEIBusiness Operations
Navajo Manufacturing Company Inc.136941411relabel(67751-162) , repack(67751-162)

Revised: 3/2023
Document Id: f6f79fd3-55a5-4d2a-e053-6394a90a4ddd
Set id: 76e32e66-4af5-47a5-83ff-cbba206975d6
Version: 3
Effective Time: 20230315
 
Navajo Manufacturing Company Inc.