FDA.reportPublic FDA data

YYBA (as PLD) - PINRID (TABLET) (73581-107)

Manufacturer
YYBA CORP
Effective date
2024-01-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:15:29

Label at a glance#

ProductPINRID
Active ingredientPYRANTEL PAMOATE
Label structure10 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

PYRANTEL PAMOATE 720.5 MG

PURPOSE

OTC - PURPOSE SECTION

PINROOM TREATMENT

USE

INDICATIONS & USAGE SECTION

FOR THE TREATMENT OF PINWORMS

WARNINGS

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions_Pinrid_12ctDirections_Pinrid_12ct

OTHER INFORMATION

OTHER SAFETY 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

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

CALL TOLL FREE 1-866-933-6337

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Pinrid_12ct01b LBL_Pinrid_12ct

01b LBL_Pinrid_24ct01b LBL_Pinrid_24ct

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73581-107PINRID (PYRANTEL PAMOATE) TABLET [YYBA CORP]3Legacy NDC20240110_94d557d7-502d-4668-b3f7-ff6591c22665.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73581-10773581-107-12, 73581-107-24

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ASPARTAMEZ0H242BBR1IACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
CROSCARMELLOSE SODIUMM28OL1HH48IACT
DEXTROSEIY9XDZ35W2IACT
FD&C YELLOW NO. 5I753WB2F1MIACT
MAGNESIUM STEARATE70097M6I30IACT
MALTODEXTRIN7CVR7L4A2DIACT
SORBITOL506T60A25RIACT
STEARIC ACID4ELV7Z65APIACT
PYRANTEL PAMOATE81BK194Z5MACTIM

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
52a6e8fb-9666-343c-e063-6294a90abdc794d557d7-502d-4668-b3f7-ff6591c226652026-05-25WarningsExact identifier
spl set id: 94d557d7-502d-4668-b3f7-ff6591c22665

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.