GEWORIN- acetaminophen, isopropylantipyrine tablet

GEWORIN by

Drug Labeling and Warnings

GEWORIN by is a Otc medication manufactured, distributed, or labeled by Lydia Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Acetaminophen, Isopropylantipyrine

PURPOSE

relief of: Headaches, Aches, Pain and Fever

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

■ 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

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

cellulose, corn starch, magnesium stearate, sodium starch glycolate

DOSAGE & ADMINISTRATION

for oral use

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GEWORIN 
acetaminophen, isopropylantipyrine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72988-0036
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	300 mg
PROPYPHENAZONE (UNII: OED8FV75PY) (PROPYPHENAZONE - UNII:OED8FV75PY)	PROPYPHENAZONE	150 mg

Inactive Ingredients
Ingredient Name	Strength
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	pink	Score	no score
Shape	TRIANGLE	Size	13mm
Flavor		Imprint Code	GR
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72988-0036-1	10 in 1 PACKAGE; Type 0: Not a Combination Product	02/11/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/11/2023

Labeler - Lydia Co., Ltd. (695735569)

Registrant - Lydia Co., Ltd. (695735569)

Establishment
Name	Address	ID/FEI	Business Operations
Lydia Co., Ltd.		695735569	manufacture(72988-0036)