Hand Sanitizer Gel

Manufacturer: Resource One Inc
Effective date: 2020-11-04
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:32:58

Label at a glance#

ProductHand Sanitizer Gel

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

Hand sanitizer to help reduce the bacteria that potentially will cause disease

Dosage and administration

Wet hands thoroughly with product and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using this product

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose:

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce the bacteria that potentially will cause disease

Warnings:

WARNINGS SECTION

For External Use Only
Flammable keep away from children

When using this product:

OTC - WHEN USING SECTION

Avoid contact with face, eyes, and broken skin. If eye contact occurs, flush thoroughly with water and seek medical advise.

Stop and ask a doctor if:

OTC - STOP USE SECTION

Irritation and redness develops

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:

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub into skin until dry.
Children under 6 years of age should be supervised by an adult when using this product

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Glycerin, Carbomer

Package Labeling: 946 ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Package Labeling:3785ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

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
77188-002-01	2023-01-30	C162847	48780-1	f386c64a-010f-0266-e053-dadaa90a7c1a	Hand Sanitizer Gel
77188-002-32	2023-01-30	C162847	48780-1	f386c64a-010f-0266-e053-dadaa90a7c1a	Hand Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77188-002-01	Hand Sanitizer Gel	3785 mL in 1 BOTTLE	GEL	3785		2
77188-002-32	Hand Sanitizer Gel	946 mL in 1 BOTTLE	GEL	946		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77188-002	HAND SANITIZER GEL (ALCOHOL) GEL [RESOURCE ONE INC]	2	Legacy NDC, 2 package rows	20201105_a93b0add-aa12-6d7f-e053-2995a90a8d07.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Hand Sanitizer Gel
ALCOHOL
GLYCERIN
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77188-002	77188-002-32, 77188-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	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
b34c4187-1fe7-347a-e053-2995a90ae548			a93b0add-aa12-6d7f-e053-2995a90a8d07	2020-11-04	Warnings	Exact identifier spl id: b34c4187-1fe7-347a-e053-2995a90ae548 spl set id: a93b0add-aa12-6d7f-e053-2995a90a8d07

Reported adverse events (FAERS/openFDA)#

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