Antimicrobial Hand Sanitizer Gel alcohol gel

Manufacturer: Hanover Pen Corp dba HPC Global | Robert Houghland
Effective date: 2020-01-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:03:23

Label at a glance#

ProductAntimicrobial Hand Sanitizer

Active ingredientALCOHOL

Label structure6 sections

Indications and uses

For handwashing to decrease bacteria on skin. Recommended for repeated use.

Dosage and administration

wet hands thoroughly with product allow to dry without wiping. children under six should be supervised while using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ehtyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on skin.
Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

OTC - DO NOT USE SECTION

Do not use in the eyes, if this happens rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product allow to dry without wiping.
children under six should be supervised while using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

aloe vera, carbomer, purified water, triethanolamine

Pkgd by HPC Global, Hanover PA, 17331

Made in USA 0.50 fl. oz. Lot# ****

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug Facts

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51811-415-40	2022-01-28	C162847	48780-1	d6a99b39-6c80-a426-e053-dadaa90af4c2	Antimicrobial Hand Sanitizer Gel alcohol gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51811-415-40	Antimicrobial Hand Sanitizer	14.79 mL in 1 BOTTLE, PLASTIC	GEL	14.79		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51811-415	ANTIMICROBIAL HAND SANITIZER (ALCOHOL RUB) GEL [HANOVER PEN CORP DBA HPC GLOBAL]	1	Legacy NDC, 1 package rows	20200123_9cbe7666-e0a3-54fb-e053-2995a90a63fb.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Antimicrobial Hand Sanitizer
Alcohol Rub
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
ALOE VERA LEAF
WATER
TROLAMINE
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51811-415	51811-415-40

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
WATER	059QF0KO0R	IACT
TROLAMINE	9O3K93S3TK	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
9cbe7666-e0a4-54fb-e053-2995a90a63fb			9cbe7666-e0a3-54fb-e053-2995a90a63fb	2020-01-22	Warnings	Exact identifier spl id: 9cbe7666-e0a4-54fb-e053-2995a90a63fb spl set id: 9cbe7666-e0a3-54fb-e053-2995a90a63fb

Reported adverse events (FAERS/openFDA)#

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