Hand Sanitizer

Manufacturer: Mansfield-King, LLC
Effective date: 2020-11-05
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:33:03

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Indications and uses

To decrease bacteria on the skin that can cause disease. Recommended for repeated use.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Storage and handling

Flammable; keep away from fire or flame.

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that can cause disease. Recommended for repeated use.

Do not use

OTC - DO NOT USE SECTION

Do not inhale or ingest.

When using

OTC - WHEN USING SECTION

When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

Directions.

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

STORAGE AND HANDLING SECTION

Flammable; keep away from fire or flame.

Inactive ingredients.

INACTIVE INGREDIENT SECTION

Water (Aqua), Aloe Barbadensis (Aloe Vera) Leaf Juice, Glycerin Tocopheryl Acetate (Vitamin E), Carbomer, Aminomethyl Propanol

Active Ingredient.

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 71%

Warnings.

WARNINGS SECTION

For external use only; hands. Flammable; keep away from fire or flame.

237ml NDC 73827-233-08

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sanilogy 237ml label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73827-233-08	2022-01-28	C162847	48780-1	d6a99b39-63fd-a426-e053-dadaa90af4c2	a627a0ed-22a9-6b46-e053-2995a90a8a4e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73827-233-08	Hand Sanitizer	237 mL in 1 BOTTLE, PLASTIC	GEL	237		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73827-233	HAND SANITIZER GEL [MANSFIELD-KING, LLC]	3	Legacy NDC, 1 package rows	20201106_a627a0ed-22a9-6b46-e053-2995a90a8a4e.zip

Products#

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

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

Hand Sanitizer
AMINOMETHYLPROPANOL
ALOE VERA LEAF
ALPHA-TOCOPHEROL ACETATE
WATER
CARBOMER INTERPOLYMER TYPE A (55000 CPS)
ALCOHOL
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73827-233	73827-233-08

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
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALPHA-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
WATER	059QF0KO0R	IACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)	59TL3WG5CO	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
b35e4c12-154e-e495-e053-2995a90a304f			a627a0ed-22a9-6b46-e053-2995a90a8a4e	2020-11-05	Warnings	Exact identifier spl id: b35e4c12-154e-e495-e053-2995a90a304f spl set id: a627a0ed-22a9-6b46-e053-2995a90a8a4e

Reported adverse events (FAERS/openFDA)#

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