Vaporal sanitizer spray

Manufacturer: Operfel S.A.
Effective date: 2020-09-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:16:31

Label at a glance#

ProductVaporal sanitizer

Active ingredientALCOHOL

Label structure6 sections

Dosage and administration

Apply on hands

Label contents#

Full prescribing information#

Active ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

For hand sanitizing decrease bacteria on the skin. Recomended for repeated use. For wound sanitizing to help prevent bacterial contamination in cuts, scrapes, burns, lacerations and skin infections.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

In children younger than 2 months of age
On open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions to use

DOSAGE & ADMINISTRATION SECTION

Apply on hands

Inactive ingredients

INACTIVE INGREDIENT SECTION

Polysorbate 20, Glycerin, PEG-7 Glyceryl Cocoate, Eucalyptol, Chlorhexidine Digluconate, Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Vaporal sanitizer
ALCOHOL
POLYSORBATE 20
GLYCERIN
PEG-7 GLYCERYL COCOATE
EUCALYPTOL
CHLORHEXIDINE GLUCONATE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79980-005	79980-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POLYSORBATE 20	7T1F30V5YH	IACT
GLYCERIN	PDC6A3C0OX	IACT
PEG-7 GLYCERYL COCOATE	VNX7251543	IACT
EUCALYPTOL	RV6J6604TK	IACT
CHLORHEXIDINE GLUCONATE	MOR84MUD8E	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	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
0e11c18d-29ac-1a43-e063-6294a90a8929			ae411677-77bc-0e37-e053-2995a90ae952	2024-01-03	Warnings	Exact identifier spl set id: ae411677-77bc-0e37-e053-2995a90ae952

Reported adverse events (FAERS/openFDA)#

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