Label at a glance#

ProductDenatured Alcohol

Active ingredientALCOHOL

Label structure11 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin.

WARNING

WARNINGS SECTION

Flammable liquid - Keep away from heat, spark, electrical, fire or flame.

Keep out of reach of children.

OTC - DO NOT USE SECTION

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - WHEN USING SECTION

When using this product,

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask doctor if irrtation or rash appears and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Conter right away.

OTC - STOP USE SECTION

Stop use and ask doctor if irrtation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Conter right away.

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly spread on both hands.

Children under 6 years of age should be supervised when using this product.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Purified Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

003-S1003

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1047755	ethanol 0.75 ML/ML Topical Solution	ethanol 0.75 ML/ML Topical Solution	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1047755	ethanol 75 % Topical Solution	PSN	2
1047755	ethanol 0.75 ML/ML Topical Solution	SCD	2
1047755	ethanol 75 % Topical Solution	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74047-003-03	2025-01-30	C162847	48780-1	2cef2736-5b41-d83d-e063-dadaa90ab31f	74047-003 Denatured Alcohol
74047-003-32	2025-01-30	C162847	48780-1	2cef2736-5b41-d83d-e063-dadaa90ab31f	74047-003 Denatured Alcohol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74047-003-03	Denatured Alcohol	38 mL in 1 BOTTLE, SPRAY	LIQUID	38		2
74047-003-32	Denatured Alcohol	3780 mL in 1 BOTTLE	LIQUID	3780		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74047-003	DENATURED ALCOHOL (ETHANOL) LIQUID [SHANTOU KANGJIE DAILY CHEMICAL INDUSTRY CO.,LTD]	2	2 package rows	20230709_fd5f7cfa-0602-ae9a-e053-6294a90aaed1.zip

Products#

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

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

Denatured Alcohol
Ethanol
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74047-003	74047-003-32, 74047-003-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
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
fff2fe2f-198c-f85f-e053-6294a90a54f5			fd5f7cfa-0602-ae9a-e053-6294a90aaed1	2023-07-08	Warnings	Exact identifier spl id: fff2fe2f-198c-f85f-e053-6294a90a54f5 spl set id: fd5f7cfa-0602-ae9a-e053-6294a90aaed1

Reported adverse events (FAERS/openFDA)#

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

Denatured Alcohol