ZEROQ FOOD

Manufacturer: JISANG Co., Ltd.
Effective date: 2020-09-28
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:30:25

Label at a glance#

ProductZEROQ FOOD

Active ingredientPOTASSIUM CARBONATE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

potassium carbonate

INACTIVE INGREDIENT SECTION

e-polylysine, dextrin, 1,2-propanediol, citric acid, tea catechin, hydroxypropylmethyl cellulose, water

OTC - PURPOSE SECTION

Helps to kill bacteria and germs on foods, and remove harmful residues on meats and vegetables.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

For hygienic disinfection, this product can be used directly to the surface. Also, you can dilute one part product with two parts water.

WARNINGS SECTION

Use only according to instruction

When using this product

Avoid direct sunlight, keep in cool place.

Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
80643-0004-1	2022-01-28	C162847	48780-1	d6a99b39-b063-a426-e053-dadaa90af4c2	b0622ed7-103c-96fd-e053-2a95a90a5add

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80643-0004-1	ZEROQ FOOD	500 mL in 1 BOTTLE, SPRAY	LIQUID	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80643-0004	ZEROQ FOOD (POTASSIUM CARBONATE) LIQUID [JISANG CO., LTD.]	1	Legacy NDC, 1 package rows	20200929_b0622ed7-103c-96fd-e053-2a95a90a5add.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

ZEROQ FOOD
Potassium carbonate
PROPYLENE GLYCOL
CITRIC ACID MONOHYDRATE
HYPROMELLOSE, UNSPECIFIED
WATER
CARBONATE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80643-0004	80643-0004-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
HYPROMELLOSE, UNSPECIFIED	3NXW29V3WO	IACT
WATER	059QF0KO0R	IACT
POTASSIUM CARBONATE	BQN1B9B9HA	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
b0622edd-f839-6899-e053-2995a90add99			b0622ed7-103c-96fd-e053-2a95a90a5add	2020-09-28	Warnings	Exact identifier spl id: b0622edd-f839-6899-e053-2995a90add99 spl set id: b0622ed7-103c-96fd-e053-2a95a90a5add

Reported adverse events (FAERS/openFDA)#

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