Label at a glance#

ProductDisposable hand sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Do not store above 110°F(43° C).

INACTIVE INGREDIENT SECTION

Deionized Water，Glycerin，Propylene Glycol，Methylparaben, Phenoxyethanol

INDICATIONS & USAGE SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry. No rinsing required.

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

1.Keep away from children.
2.For external use only.
3.Keep out of eyes. If contacts eyes, flush with water and call a doctor.
4.If irritation or rash: appears and persists, stops use and see a physician.
5.Do not store above 110°F(43° C)
6.If swallowed, get medical help or contact a Poison Control Center right away.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1039012	Benzalkonium (Topical)	benzalkonium chloride 1.3 MG/ML Topical Spray	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1039012	benzalkonium chloride 0.13 % Topical Spray	PSN	2
1039012	benzalkonium chloride 1.3 MG/ML Topical Spray	SCD	2
1039012	benzalkonium chloride 0.13 % Topical Spray	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55297-001-01	2022-01-28	C162847	48780-1	d6a99b39-c678-a426-e053-dadaa90af4c2	ab02746d-d329-3869-e053-2a95a90a5eff

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55297-001-01	Disposable hand sanitizer	500 mL in 1 BOTTLE	SPRAY	500		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55297-001	DISPOSABLE HAND SANITIZER (ALCOHOL FREE HAND SANITIZER) SPRAY [NINGBO SALIX HYGIENE PRODUCTS CO., LTD.]	2	Legacy NDC, 1 package rows	20200807_ab02746d-d329-3869-e053-2a95a90a5eff.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Disposable hand sanitizer
ALCOHOL FREE HAND SANITIZER
WATER
GLYCERIN
METHYLPARABEN
BENZALKONIUM CHLORIDE
BENZALKONIUM
PROPYLENE GLYCOL
PHENOXYETHANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55297-001	55297-001-01

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
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
METHYLPARABEN	A2I8C7HI9T	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
PROPYLENE GLYCOL	6DC9Q167V3	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT

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
ac405ad6-29ce-109a-e053-2995a90a9051			ab02746d-d329-3869-e053-2a95a90a5eff	2020-08-06	Warnings	Exact identifier spl id: ac405ad6-29ce-109a-e053-2995a90a9051 spl set id: ab02746d-d329-3869-e053-2a95a90a5eff

Reported adverse events (FAERS/openFDA)#

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

Disposable hand sanitizer