VG-70HS-70C Handsanitizer

Manufacturer: Sharp International Services, LLC
Effective date: 2020-08-10
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:24:18

Label at a glance#

ProductVG-70HS-70C Handsanitizer HANDSANITIZER

Active ingredientALCOHOL

Label structure11 sections

Storage and handling

Store between 15 - 30C (59 - 86 F) Avoidfreezing and storage above 40C (140F)

Label contents#

Full prescribing information#

Drug Active

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients	Purpose
Ethyl Alcohol 70%v/v	Antiseptic

OTC - WHEN USING SECTION

Uses:

Hand sanitizer to help reduce bacteria that potentially can cause disease.
For use when soap and water are not available.

OTC - ASK DOCTOR SECTION

Stop Use amd ask a doctor if

irritation or rash occurs
condition persists for more than 72 hours

OTC - DO NOT USE SECTION

Do not use

For children less than 2 months of age
on open skin wounds

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

If swallowed, get medical help, or contact a Posion ControlCenter Right Away

OTC - PURPOSE SECTION

Uses:

Handsanitizer to help reduce bacteria that potentially can cause disease. For use when soap and wateer are not available

WARNINGS SECTION

Warnings

For external use only : hands
Flammable keep away from heat or flame
Do not ingest or inhale

OTC - STOP USE SECTION

Stop use and ask a doctor if

irritation or rash occurs
condition persists for more than 72 hours

STORAGE AND HANDLING SECTION

Store between 15 - 30C (59 - 86 F)
Avoidfreezing and storage above 40C (140F)

INACTIVE INGREDIENT SECTION

Fragrance

Glycerin

PEG-6 and AMP - Acrylatees/ Vinyl Isodecanoate Crosspolymer

Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VG 70 - 275 Gal Tote

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	2
581662	ethanol 0.7 ML/ML Topical Gel	SCD	2
581662	ethanol 70 % Topical Gel	SY	2
581662	ethyl alcohol 70 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74221-006-03	2022-01-28	C162847	48780-1	d6a99b39-9332-a426-e053-dadaa90af4c2	VG-70 HANDSANITIZER SHARP INTERNATIONAL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74221-006-03	VG-70HS-70C HandsanitizerHANDSANITIZER	1003 L in 1 CONTAINER	GEL	1003		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74221-006	VG-70HS-70C HANDSANITIZER HANDSANITIZER (ALCOHOL) GEL [SHARP INTERNATIONAL SERVICES, LLC]	2	Legacy NDC, 1 package rows	20200811_ac61cdc1-2e18-521b-e053-2a95a90a82a1.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

VG-70HS-70C Handsanitizer HANDSANITIZER
ALCOHOL
WATER
GLYCERIN
RAPIDGEL EZ1

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74221-006	74221-006-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
RAPIDGEL EZ1	33JH4A7R2K	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
ac8d6829-a4a3-0df0-e053-2a95a90ab945			ac61cdc1-2e18-521b-e053-2a95a90a82a1	2020-08-10	Warnings	Exact identifier spl id: ac8d6829-a4a3-0df0-e053-2a95a90ab945 spl set id: ac61cdc1-2e18-521b-e053-2a95a90a82a1

Reported adverse events (FAERS/openFDA)#

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