Label at a glance#

ProductWET WIPES

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry Supervise children under 6 years old Not recommended for repeats

Storage and handling

Store at 15-30℃

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizer to reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep product away from fire or flame.

When using this product

OTC - WHEN USING SECTION

When using this product keep away from eyes.In case of contact,rinse eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry
Supervise children under 6 years old
Not recommended for repeats

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water

Other informations

STORAGE AND HANDLING SECTION

Store at 15-30℃

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

150 PCS IN 1 PAIL NDC: 78736-003-01

Label

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1307051	Ethanol (Topical)	ethanol 0.75 ML/ML Medicated Pad	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1307051	ethanol 75 % Medicated Pad	PSN	1
1307051	ethanol 0.75 ML/ML Medicated Pad	SCD	1
1307051	ethanol 75 % Hand Sanitizer Wipes	SY	1
1307051	ethyl alcohol 75 % Topical Cloth	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78736-003-01	2022-01-28	C162847	48780-1	d6a99b39-ae29-a426-e053-dadaa90af4c2	WET WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78736-003-01	WET WIPES	1 g in 1 NOT APPLICABLE	CLOTH	1		1
78736-003-01	WET WIPES	150 in 1 PAIL	CLOTH	150		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78736-003	WET WIPES (75% ALCOHOL ANTISEPTIC WIPES) CLOTH [HUANGSHAN NANGUOZHICHUN TOURISTS PRODUCTS CO., LTD.]	1	Legacy NDC, 2 package rows	20200812_ac8a2eb1-12c3-5526-e053-2995a90a3e40.zip

Products#

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

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

WET WIPES
75% Alcohol Antiseptic wipes
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78736-003	78736-003-01

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
ac8a252b-4248-5e2c-e053-2a95a90acd54			ac8a2eb1-12c3-5526-e053-2995a90a3e40	2020-08-10	Warnings	Exact identifier spl id: ac8a252b-4248-5e2c-e053-2a95a90acd54 spl set id: ac8a2eb1-12c3-5526-e053-2995a90a3e40

Reported adverse events (FAERS/openFDA)#

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

WET WIPES