Hand Sanitizer

Manufacturer: Prostat First Aid LLC
Effective date: 2025-12-15
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 01:23:05

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure9 sections

Dosage and administration

Wet hand thoroughly with product and allow to dry without wiping

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact1-888-900-2920

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic Handwash

Use(s)

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For External Use Only

Flammable. Keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

In the eyes

When using this product

OTC - WHEN USING SECTION

• Avoid contact with eyes

• In case of eye contact, rinse with water to remove

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation and redness develop

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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hand thoroughly with product and allow to dry without wiping

Other Information

OTHER SAFETY INFORMATION

• Do not store above 110•F (43ºC)

• May discolor some fabrics

• Recommended for repeated use

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera Leaf Extract, Carbopol Ultrez 10, Fragrance, Glycerin, Propylene Glycol, Purified Water, Triethanolamine

Questions?

OTC - QUESTIONS SECTION

1-888-900-2920 Monday-Friday 8AM-4PM PST.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PS-0691_IN_MASTER

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	3
581662	ethanol 0.7 ML/ML Topical Gel	SCD	3
581662	ethanol 70 % Topical Gel	SY	3
581662	ethyl alcohol 70 % Topical Gel	SY	3

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0814889013989	GTIN-13: 0814889013989 EAN-13: 0814889013989 GTIN-12: 814889013989 UPC-A: 814889013989 GTIN storage (14 digits): 00814889013989	PS-0691_IN_MASTER_R231130-1.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58228-0691-1	Hand Sanitizer	6 in 1 BAG	GEL	6		3
58228-0691-1	Hand Sanitizer	1200 in 1 CASE	GEL	1200		3

Products#

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

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

Hand Sanitizer
ALOE VERA LEAF
ALCOHOL
WATER
PROPYLENE GLYCOL
GLYCERIN
TROLAMINE
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58228-0691	58228-0691-1

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
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
GLYCERIN	PDC6A3C0OX	IACT
TROLAMINE	9O3K93S3TK	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	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
Hand Sanitizer	HAND SANITIZER	Prostat First Aid LLC	0e241343-db64-3f1c-e063-6394a90ab538	2025-12-15	Warnings	Exact identifier ndc (package): 58228-0691-1 ndc (product): 58228-0691 ndc11 (package): 58228069101 spl id: 46016372-2d5b-d2d6-e063-6294a90af984 spl set id: 0e241343-db64-3f1c-e063-6394a90ab538

Reported adverse events (FAERS/openFDA)#

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