Comfort

Manufacturer: WEIMEI Lianyungang HOUSEHOLD ARTICLES MANUFACTURING CO.LTD
Effective date: 2014-01-03
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:38:14

Label at a glance#

ProductComfort

Active ingredientISOPROPYL ALCOHOL

Label structure8 sections

Indications and uses

Help Prevent the risk of infection in Minor Cuts - Scrapes - Burns

Dosage and administration

Clean affected area - apply a small amount of product 1 to 3 times a day

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 50%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

Help Prevent the risk of infection in Minor Cuts - Scrapes - Burns

Warnings

WARNINGS SECTION

For External Use Only

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

Ask a doctor before use if ou have deep or punture wound, animal bites or serious burns

Stop use and ask doctor if the condition persisits or gets worse

When using this product, do not get into eyes do not apply over large areas of the body

do not use longer than a week

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a posion control center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

Clean affected area - apply a small amount of product 1 to 3 times a day

Other Information

OTHER SAFETY INFORMATION

does not contain nor is intened as substitute for grain or ethyl alcohol. will produce serious gastric disturbances if taken internally

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcoholimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616456	isopropyl alcohol 50 % Topical Solution	PSN	1
616456	isopropyl alcohol 0.5 ML/ML Topical Solution	SCD	1
616456	isopropyl alcohol 50 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50827-002-83	2019-11-27	C162847	48780-1	9855e2a2-3cf3-60a7-e053-dbdaa90a05bd	ecd4b358-bc5d-4d21-a82a-7b3809ce8ee9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50827-002-83	Comfort	354 mL in 1 BOTTLE, PLASTIC	LIQUID	354		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50827-002	COMFORT (ALCOHOL) LIQUID [WEIMEI LIANYUNGANG HOUSEHOLD ARTICLES MANUFACTURING CO.LTD]	1	Legacy NDC, 1 package rows	20140129_ecd4b358-bc5d-4d21-a82a-7b3809ce8ee9.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ISOPROPYL ALCOHOL	ACTIVE INGREDIENT	ND2M416302	1
ISOPROPYL ALCOHOL	ACTIVE MOIETY	ND2M416302	1
Water	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

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

Comfort
Alcohol
ISOPROPYL ALCOHOL
Water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50827-002	50827-002-83

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
ISOPROPYL ALCOHOL	ND2M416302	ACTIB
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
2910b512-cc87-449b-9529-5e72528df5a3			ecd4b358-bc5d-4d21-a82a-7b3809ce8ee9	2014-01-03	Warnings	Exact identifier spl id: 2910b512-cc87-449b-9529-5e72528df5a3 spl set id: ecd4b358-bc5d-4d21-a82a-7b3809ce8ee9

Reported adverse events (FAERS/openFDA)#

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