PARASITOL- pyrantel pamoate suspension

PARASITOL by

Drug Labeling and Warnings

PARASITOL by is a Otc medication manufactured, distributed, or labeled by Menper Distributors Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS

PYRANTEL PAMOATE 144 MG/ML

PURPOSE

PURPOSE

PARASITICIDE

INDICATIONS & USAGE

USES

FOR THE TREATMENT OF PINWORMS.

WARNINGS

WARNINGS

ABDOMINAL CRAMPS, NAUSEA, VOMITING, DIARRHEA HEADACHES OR DIZZINESS SOMETIMES OCCUR AFTER TAKING THIS DRUG. IF ANY OF THOSE CONDITIONS PERSIST, CONSULT A DOCTOR. IF YOU ARE PREGNANT OR HAVE LIVER DISEASE, DO NOT TAKE THIS PRODUCT UNLESS DIRECTED BY A DOCTOR. PROTECT FROM EXCESSIVE HEAT AND FREEZING. SHAKE WELL.

STORE AT CONTROLLED ROOM TEMPERATURE.

READ WARNINGS AND PACKAGE INSERT CAREFULLY BEFORE TAKING THIS MEDICATION.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

DOSAGE & ADMINISTRATION

DIRECTIONS

ADULTS AND CHILDREN 12 YEARS OF AGE AND OVER AND CHILDREN 2 YEARS OF AGE TO UNDER TWELVE YEARS, ORAL DOSAGE IS A SINGLE DOSE OF 5MG OF PARASITOL PER POUND OR 11 MG PER KG OFBODY WEIGHT, NOT TO EXCEED 1 GM. TAKE ONLY ACCORDING TO DIRECTIONS AND DO NOT EXCEED RECOMMENDED DOSGE UNLESS DIRECTED BY A DOCTOR. MEDICATION SHOULD ONLY BE TAKEN ONE TIME AS A SINGLE DOSE. DO NOT REPEAT TREATMENT UNLESS DIRECTED BY A DOCTOR. WHEN ONE INDIVIDUAL IN HOUSEHOLD HAS PARSITES, THE ENTIRE HOUSEHOLD SHOULD BE TREATED UNLESS OTHERWISE ADVISED.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS

PURIFIED WATER, SUCROSE, PROPYLENE GLYCOL, SODIUM CARBOXYMETHYLCELLULOSE, XANTHAN GUM, METHYLPARABEN, CHERRY FLAVOR AND PROPYLPARABEN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PARASITOL 
pyrantel pamoate suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53145-101
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRANTEL PAMOATE (UNII: 81BK194Z5M) (PYRANTEL - UNII:4QIH0N49E7)	PYRANTEL	144 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
WATER (UNII: 059QF0KO0R)
SUCROSE (UNII: C151H8M554)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53145-101-11	1 in 1 BOX
1	NDC: 53145-101-01	30 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part357B	01/01/2013

Labeler - Menper Distributors Inc. (101947166)