Hand Saniter Mist

Manufacturer: Hand Saniter Mist-32519746 | ZHEJIANG GAORONG COSMETICS CO., LTD
Effective date: 2025-04-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:01:56

Label at a glance#

ProductHand Saniter Mist

Active ingredientDEHYDRATED ALCOHOL

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1041849	ethanol 70 % Topical Spray	PSN	1
1041849	ethanol 0.7 ML/ML Topical Spray	SCD	1
1041849	ethanol 70 % Topical Spray	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69933-746-12	Hand Saniter Mist	1 mL in 1 BOTTLE, PLASTIC	LIQUID	1		1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Hand Saniter Mist
DEHYDRATED ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69933-746	69933-746-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DEHYDRATED ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	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
335c0636-3c1f-e742-e063-6294a90ad4dc			335c0636-3c1e-e742-e063-6294a90ad4dc	2025-04-22		Exact identifier spl id: 335c0636-3c1f-e742-e063-6294a90ad4dc spl set id: 335c0636-3c1e-e742-e063-6294a90ad4dc

Reported adverse events (FAERS/openFDA)#

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