GEWORIN

Manufacturer
Lydia Co., Ltd.
Effective date
2023-08-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:55:51

Label at a glance#

ProductGEWORIN
Active ingredientACETAMINOPHEN, PROPYPHENAZONE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen, Isopropylantipyrine

OTC - PURPOSE SECTION

relief of: Headaches, Aches, Pain and Fever

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

■ adult and children 15 years of age and older: 1 capsules three times a day

■ children under 15 years of age: ask a doctor

WARNINGS SECTION

Warnings

Do not use if carton is open or if printed bottle neck band or inner foil seal is broken.physician

Keep out of the reach of children. This package contains enough drug to seriously harm a child. Do not use with other drugs containing acetaminophen.

Use the smallest effective dose. Do not take more than the maximum daily dose. Overdose may result in severe or possibly fatal liver damage.

Do not take if allergic to acetaminophen. Consult a doctor if: your symptoms last for more than 5 days or fever lasts more than 3 days or you develop allergic reactions such as wheezing, rash or itching.

Ask a doctor or pharmacist before use if you: Are pregnant or breastfeeding, have chronic alcoholism; have a serious liver or kidney disease; use any other medications including natural health products, prescription drugs, salicylates or other pain and fever relief medications.

In case of overdose, call a Poison Control Centre or doctor immediately, even if you do not notice any possible signs or symptoms such as increased sweating, nausea, vomiting, stomach pain, and loss of appetite.

INACTIVE INGREDIENT SECTION

cellulose, corn starch, magnesium stearate, sodium starch glycolate

DOSAGE & ADMINISTRATION SECTION

for oral use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72988-0036-1GEWORIN10 in 1 PACKAGETABLET103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72988-0036GEWORIN (ACETAMINOPHEN, ISOPROPYLANTIPYRINE) TABLET [LYDIA CO., LTD.]3Current NDC, 1 package rows20230809_f46826d8-fdef-bfaf-e053-2a95a90aa89e.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72988-003672988-0036-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

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
GEWORINACETAMINOPHEN, ISOPROPYLANTIPYRINELydia Co., Ltd.f46826d8-fdef-bfaf-e053-2a95a90aa89e2023-08-09WarningsExact identifier
ndc (package): 72988-0036-1
ndc (product): 72988-0036
ndc11 (package): 72988003601
spl id: 0278e810-7614-f9e0-e063-6394a90a3198
spl set id: f46826d8-fdef-bfaf-e053-2a95a90aa89e

Reported adverse events (FAERS/openFDA)#

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