ZEROQ FACE BODY

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 23:30:24

Label at a glance#

ProductZEROQ FACE BODY

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

Sanitizer to help decrease bacteria on skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Spray on skin as needed

WARNINGS SECTION

For external use only.

When using this product

Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear.

Keep out of reach of children.

Store at room temperature.

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
80643-0003-1	2022-01-28	C162847	48780-1	d6a99b39-b060-a426-e053-dadaa90af4c2	b062193f-b59a-0b02-e053-2995a90a6b88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80643-0003-1	ZEROQ FACE BODY	100 mL in 1 BOTTLE, SPRAY	LIQUID	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80643-0003	ZEROQ FACE BODY (POTASSIUM CARBONATE) LIQUID [JISANG CO., LTD.]	1	Legacy NDC, 1 package rows	20200929_b062193f-b59a-0b02-e053-2995a90a6b88.zip

Products#

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

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80643-0003	80643-0003-1

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
b061fcf0-af92-96ff-e053-2a95a90a99fc			b062193f-b59a-0b02-e053-2995a90a6b88	2020-09-28	Warnings	Exact identifier spl id: b061fcf0-af92-96ff-e053-2a95a90a99fc spl set id: b062193f-b59a-0b02-e053-2995a90a6b88

Reported adverse events (FAERS/openFDA)#

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