PINRID- pyrantel pamoate tablet

PINRID by

Drug Labeling and Warnings

PINRID by is a Otc medication manufactured, distributed, or labeled by YYBA CORP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

PYRANTEL PAMOATE 720.5 MG

PURPOSE

PINROOM TREATMENT

USE

FOR THE TREATMENT OF PINWORMS

WARNINGS

IF ANY OF THESE CONDITIONS PERSIST, CONSULT A DOCTOR

• DIZZINESS
• DIARHEA
• ABDOMINAL CRAMPS
• VOMITING
• NAUSEA
• HEADACHE

IF PREGNANT OR IF YOU HAVE LIVER DISEASE, ASK A DOCTOR BEFORE USE. CONSULT YOUR DOCTOR IF AN ALLERGIC REACTION OCCURS.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. IN CASE OF ACCIDENTAL OVERDOSE, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS FOR USE

OTHER INFORMATION

• PHENYLKETONURICS: CONTAIN PHENYLALANINE 11.8 MG PER TABLET
• READ PACKAGE INSERT CAREFULLY BEFORE USING
• IF SIGNS OF PINWORMS PERSIST, SEE A DOCTOR
• STORE AT 15° - 30°c (59° - 86°f)

INACTIVE INGREDIENTS

aspartame powder, citric acid, colloidal silicon dioxide, croscarmellose sodium, dextrose, FD&C yellow, magnesium stearate, maltodextrin, sorbitol, stearic acid, orange fl avor.

QUESTIONS OR COMMENTS?

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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PINRID 
pyrantel pamoate tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73581-107
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRANTEL PAMOATE (UNII: 81BK194Z5M) (PYRANTEL - UNII:4QIH0N49E7)	PYRANTEL	250 mg

Inactive Ingredients
Ingredient Name	Strength
ASPARTAME (UNII: Z0H242BBR1)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
DEXTROSE (UNII: IY9XDZ35W2)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SORBITOL (UNII: 506T60A25R)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	11mm
Flavor		Imprint Code	WM1
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73581-107-12	12 in 1 BOTTLE; Type 0: Not a Combination Product	04/02/2021
2	NDC: 73581-107-24	24 in 1 BOTTLE; Type 0: Not a Combination Product	04/02/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M031	04/02/2021

Labeler - YYBA CORP (006339772)