Lombrix

Manufacturer
OPMX LLC
Effective date
2026-09-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-10-06 02:03:58

Label at a glance#

ProductLombrix
Active ingredientPYRANTEL PAMOATE
Label structure11 sections

Storage and handling

Other information: store at 15°-30°C (59°-86°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each uncoated tablet)

Pyrantel Pamoate USP 180 mg (equivalent to 62.5mg of pyrantel base)

OTC - PURPOSE SECTION

Purpose

Antihelmintic

INDICATIONS & USAGE SECTION

Use:for the treatment of pinworms

WARNINGS SECTION

Warnings:Do not exceed recommended dosage

OTC - ASK DOCTOR SECTION

Ask a doctor before use if:

  • you're pregnant
  • you're nursing a baby
  • you have liver disease

OTC - WHEN USING SECTION

When using this product:abdominal cramps, nausea, vomiting, diarrhea, headache, or dizziness sometimes occur after taking this drug. If any of these symptoms persist consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.In case of overdose, get medical help or contact a poison control center rightaway.

DOSAGE & ADMINISTRATION SECTION

Directions:

Adults, children 12 years of age and over, and children 2 years to under 12 years: Oral dossage is a single dose of 5 mg of pyrantel base per pound or 11 mg of pyrantel base per kilogram of body weight. Do not Exceed 1 gram (1000mg). Children Under 25lbs. or 2yrs: Don't use unless directed by a doctor.

READ PACKAGE INSERT CAREFULLY BEFORE TAKING THIS MEDICATION

WeightDosage(taken as a single dose)
Less than 25 lb. or under 2 yrs. oldDo not use unless directed by a doctor
25-37 lb.2 tablets
38-62 lb.4 tablets
63-87 lb.6 tablets
88-112 lb.8 tablets
113-137 lb.10 tablets
138-162 lb.12 tablets
163-187 lb.14 tablets
188 lb & over16 tablets

STORAGE AND HANDLING SECTION

Other information:

  • store at 15°-30°C (59°-86°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients:Colloidal silicon dioxide, croscarmellose sodium, crospovidone, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, potassium sorbate, povidone, talc.

OTHER SAFETY INFORMATION

TAMPER-EVIDENT: DO NOT USE IF THE BLISTER IS CUT OR BROKEN

SPL UNCLASSIFIED SECTION

Exclusively distributed by

OPMX

Chula Vista, CA 91910

Questions or comments:

619-600-5632

MADE IN INDIA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 69729-807-10

Lombrix

Pyrantel Pamoate Tablets 180 mg

TREATMENT FOR PINWORMS

  • Recommended By Health Care Professionals ForThe Entire Family

​10 Tablets

lolo

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130810053181768GTIN-13: 0810053181768
EAN-13: 0810053181768
GTIN-12: 810053181768
UPC-A: 810053181768
GTIN storage (14 digits): 00810053181768
-Lombrix Treatment Pinworms w10 tablets RTE REV 09.2025_001.jpg
QR code linkQR Codeopmx.us/-Lombrix Treatment Pinworms w10 tablets RTE REV 09.2025_001.jpg

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
69729-80769729-807-10

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-09-24full-release2026-06-01 01:14:50

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
LombrixPYRANTEL PAMOATEOPMX LLC3f940481-8e75-0bc7-e063-6394a90af1cd2025-09-24WarningsExact identifier
ndc (package): 69729-807-10
ndc (product): 69729-807
ndc11 (package): 69729080710
spl set id: 3f940481-8e75-0bc7-e063-6394a90af1cd

Reported adverse events (FAERS/openFDA)#

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