Hand Sanitizer

Manufacturer: Broder Bros Prime Line
Effective date: 2020-08-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:26:04

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Indications and uses

for hand sanitizing.

Dosage and administration

Wet hands thoroughly with product, brisky rub together until dry. Always supervise children in the use of this product. Children under the age of 6 months: Ask a doctor.

Contacts and useful links#

PhoneLabel contact1-800-873-7746

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

for hand sanitizing.

Warnings

WARNINGS SECTION

Flammable, keep away from fire and flame

For external use only

When using this product

OTC - WHEN USING SECTION

Keep out of eyes
In case of contact with eyes, flush thoroughly with water.
Avoid contact with broken skin.
Do not inhale or ingest.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develops and persists for more than 72 hours.

Keep our of reach of Children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product, brisky rub together until dry.
Always supervise children in the use of this product.
Children under the age of 6 months: Ask a doctor.

Other information

OTHER SAFETY INFORMATION

Store at 66 to 77 F (22 to 25 C)
May discolor some fabrics
Harmful to wood finishes and platics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Glycerin, Triethanolamine, Water

Question?

OTC - QUESTIONS SECTION

1-800-873-7746

M-F 8am-5pm EST

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

360 mL NDC: 80017-002-01

PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	1
1305100	ethanol 75 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
80017-002-01	2022-01-28	C162847	48780-1	d6a99b39-fa71-a426-e053-dadaa90af4c2	Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80017-002-01	Hand Sanitizer	360 mL in 1 BOTTLE	GEL	360		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80017-002	HAND SANITIZER (ALCOHOL) GEL [BRODER BROS PRIME LINE]	1	Legacy NDC, 1 package rows	20200828_add5887d-f97c-6134-e053-2a95a90a4eb1.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Hand Sanitizer
ALCOHOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE
WATER
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80017-002	80017-002-01
74742-008

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 HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TROLAMINE	9O3K93S3TK	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	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
add5ac88-8736-9898-e053-2995a90a75e0			add5887d-f97c-6134-e053-2a95a90a4eb1	2020-08-27	Warnings	Exact identifier spl id: add5ac88-8736-9898-e053-2995a90a75e0 spl set id: add5887d-f97c-6134-e053-2a95a90a4eb1

Reported adverse events (FAERS/openFDA)#

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