Hand Sanitizer

Manufacturer: Mastitis Management Tools, Inc.
Effective date: 2020-12-31
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:36:17

Label at a glance#

ProductHand Sanitizer

Active ingredientISOPROPYL ALCOHOL

Label structure7 sections

Indications and uses

For hand sanitizing to decrease bacteria on skin Recommended for repeated use

Dosage and administration

place a small amount into palm. rub thoroughly over all surfaces of both hands. rub hands together briskly until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on skin
Recommended for repeated use

Warning

WARNINGS AND PRECAUTIONS SECTION

For External use only.
When using this product avoid contact with eyes. in case of eye contact, flush eyes with water.
Stop use and ask doctor if irritation or redness developed, or if condition persists for more than 72 hours.
Keep out of the reach of children.
If swallowed, get medical help or contact a poison control center immediately.

For external use only.

WARNINGS SECTION

When using this product avoid contact with eyes. in case of eye contact, flush eyes with water.

WARNINGS SECTION

Stop use and ask doctor if irritation or redness developed, or if condition persists for more than 72 hours.

OTC - STOP USE SECTION

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poison control center immediately.

WARNINGS SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

place a small amount into palm.
rub thoroughly over all surfaces of both hands.
rub hands together briskly until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Deionized water, Cellulose

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2 oz Hand sanitizer labels

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581698	isopropyl alcohol 70 % Topical Gel	PSN	3
581698	isopropyl alcohol 0.7 ML/ML Topical Gel	SCD	3
581698	isopropyl alcohol 70 % Topical Gel	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73768-372-18	2022-01-28	C162847	48780-1	d6a99b3a-014c-a426-e053-dadaa90af4c2	a15133d3-ad97-b9f3-e053-2995a90ab0a3
73768-372-22	2022-01-28	C162847	48780-1	d6a99b3a-014c-a426-e053-dadaa90af4c2	a15133d3-ad97-b9f3-e053-2995a90ab0a3
73768-372-52	2022-01-28	C162847	48780-1	d6a99b3a-014c-a426-e053-dadaa90af4c2	a15133d3-ad97-b9f3-e053-2995a90ab0a3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
73768-372-18	Hand Sanitizer	0.059 L in 1 BOTTLE, PLASTIC	GEL	0.059	3
73768-372-22	Hand Sanitizer	0.118 L in 1 BOTTLE, PLASTIC	GEL	0.118	3
73768-372-52	Hand Sanitizer	3.78 L in 1 BOTTLE, PLASTIC	GEL	3.78	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73768-372	HAND SANITIZER GEL [MASTITIS MANAGEMENT TOOLS, INC.]	3	Legacy NDC, 3 package rows	20210101_a15133d3-ad97-b9f3-e053-2995a90ab0a3.zip

Products#

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

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

Hand Sanitizer
ISOPROPYL ALCOHOL
HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%)
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73768-372	73768-372-18, 73768-372-22, 73768-372-52
73749-101

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
ISOPROPYL ALCOHOL	ND2M416302	ACTIB
HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%)	ZYD53NBL45	IACT
WATER	059QF0KO0R	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
b7cc89fa-6efe-c574-e053-2995a90aff66			a15133d3-ad97-b9f3-e053-2995a90ab0a3	2020-12-31	Warnings	Exact identifier spl id: b7cc89fa-6efe-c574-e053-2995a90aff66 spl set id: a15133d3-ad97-b9f3-e053-2995a90ab0a3

Reported adverse events (FAERS/openFDA)#

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