Hand Sanitizer

Manufacturer: AAkron Rule Corporation
Effective date: 2022-07-25
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 23:50:15

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure9 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(S)

INDICATIONS & USAGE SECTION

helps reduce bacteria that can cause disease when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Do not use

in children less than 2 months of age
on open skin wounds

When using this product avoid mouth, eyes, and ears. In case of contact with eyes, flush with water .

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help and call Poison Control.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Label 2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1039339	ethanol 80 % Topical Solution	PSN	4
1039339	ethanol 0.8 ML/ML Topical Solution	SCD	4
1039339	ethanol 80 % Topical Solution	SY	4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5eb9f24b-9328-475e-af0a-18021935eb6a	Product name	1	20180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69394-001-01	2024-01-30	C162847	48780-1	d6a99b39-ae14-a426-e053-dadaa90af4c2	7ff1c2d4-3a11-4606-829e-0c8930d7c3e2
69394-001-02	2024-01-30	C162847	48780-1	d6a99b39-ae14-a426-e053-dadaa90af4c2	7ff1c2d4-3a11-4606-829e-0c8930d7c3e2
69394-001-03	2024-01-30	C162847	48780-1	d6a99b39-ae14-a426-e053-dadaa90af4c2	7ff1c2d4-3a11-4606-829e-0c8930d7c3e2
69394-001-01	2022-03-02	C162847	48780-1	d6a99b39-ae14-a426-e053-dadaa90af4c2	7ff1c2d4-3a11-4606-829e-0c8930d7c3e2
69394-001-02	2022-03-02	C162847	48780-1	d6a99b39-ae14-a426-e053-dadaa90af4c2	7ff1c2d4-3a11-4606-829e-0c8930d7c3e2
69394-001-03	2022-03-02	C162847	48780-1	d6a99b39-ae14-a426-e053-dadaa90af4c2	7ff1c2d4-3a11-4606-829e-0c8930d7c3e2
69394-001-01	2022-01-28	C162847	48780-1	d6a99b39-ae14-a426-e053-dadaa90af4c2	7ff1c2d4-3a11-4606-829e-0c8930d7c3e2
69394-001-02	2022-01-28	C162847	48780-1	d6a99b39-ae14-a426-e053-dadaa90af4c2	7ff1c2d4-3a11-4606-829e-0c8930d7c3e2
69394-001-03	2022-01-28	C162847	48780-1	d6a99b39-ae14-a426-e053-dadaa90af4c2	7ff1c2d4-3a11-4606-829e-0c8930d7c3e2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
69394-001-01	Hand Sanitizer	30 mL in 1 BOTTLE, PLASTIC	LIQUID	30	4
69394-001-02	Hand Sanitizer	89 mL in 1 BOTTLE, PLASTIC	LIQUID	89	4
69394-001-03	Hand Sanitizer	1893 mL in 1 BOTTLE, PLASTIC	LIQUID	1893	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69394-001	HAND SANITIZER (ALCOHOL) LIQUID [AAKRON RULE CORPORATION]	4	Legacy NDC, 3 package rows	20220726_7ff1c2d4-3a11-4606-829e-0c8930d7c3e2.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Hand Sanitizer
Alcohol
GLYCERIN
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69394-001	69394-001-01, 69394-001-02, 69394-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
WATER	059QF0KO0R	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
e4a2adc1-fcf5-895a-e053-2a95a90ac09b			7ff1c2d4-3a11-4606-829e-0c8930d7c3e2	2022-07-25	Warnings	Exact identifier spl id: e4a2adc1-fcf5-895a-e053-2a95a90ac09b spl set id: 7ff1c2d4-3a11-4606-829e-0c8930d7c3e2

Reported adverse events (FAERS/openFDA)#

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