Instant Hand Sanitizer

Manufacturer: KeRuiSi Cosmetics (Jinhua) Co.,Ltd.
Effective date: 2020-05-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:11:01

Label at a glance#

ProductInstant Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Store in a cool dry place.

INACTIVE INGREDIENT SECTION

AQUA

Propylene Glycol

Glycerin

CARBOMER

AMINOMETHYL PROPANOL

INDICATIONS & USAGE SECTION

apply approptiate amount of this product to The palm.rub with both hands until dry without washing.

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization

WARNINGS SECTION

1 keep out of reach of children.cont be swallowed just for External disinfectant.
2.Avoid to use together with agonist drugs.
3.Use in coution if allegric.
4.Flammable liquid.keep product away from heal.
5.Store in a cool dry place.
6.Always seals after use before Validity period.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55422-001-01	2022-01-28	C162847	48780-1	d6a99b39-577a-a426-e053-dadaa90af4c2	a56f5a49-7a4f-8b72-e053-2995a90abe4f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55422-001-01	Instant Hand Sanitizer	30 mL in 1 BOTTLE	LIQUID	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55422-001	INSTANT HAND SANITIZER LIQUID [KERUISI COSMETICS (JINHUA) CO.,LTD.]	1	Legacy NDC, 1 package rows	20200513_a56f5a49-7a4f-8b72-e053-2995a90abe4f.zip

Products#

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

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

Instant Hand Sanitizer
PROPYLENE GLYCOL
AMINOMETHYLPROPANOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
ALCOHOL
GLYCERIN
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55422-001	55422-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PROPYLENE GLYCOL	6DC9Q167V3	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT

Source Document#

Source XML · Source PDF

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
a56f5a49-7a50-8b72-e053-2995a90abe4f			a56f5a49-7a4f-8b72-e053-2995a90abe4f	2020-05-12	Warnings	Exact identifier spl id: a56f5a49-7a50-8b72-e053-2995a90abe4f spl set id: a56f5a49-7a4f-8b72-e053-2995a90abe4f

Reported adverse events (FAERS/openFDA)#

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