20 pack Alcohol Hand Wipes-Fresh

Manufacturer: Zhuji Jianhe Paper Co., Ltd
Effective date: 2020-09-23
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:30:04

Label at a glance#

Product20 pack Alcohol Hand Wipes-Fresh

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry. Children under 6 years of age should be supervised when using product.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethanol Alcohol 75% v/v. Purpose: Antibacterial

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

Decreases bacteria on skin.

Warnings

WARNINGS SECTION

For external use only.
Keep away from fire or flame

When using

OTC - WHEN USING SECTION

When using this product keep out of eyes. If contact with eyes occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation 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 Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry.
Children under 6 years of age should be supervised when using product.

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

Water, Fragrance.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20 CLOTH IN 1 PACKAGE NDC: 75163-020-20

20 CLOTH LABEL

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
75163-020-20	2022-01-28	C162847	48780-1	d6a99b39-62b6-a426-e053-dadaa90af4c2	75163-020 20 pack Alcohol Hand Wipes-Fresh jianhe 20200923

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75163-020-20	20 pack Alcohol Hand Wipes-Fresh	20 in 1 PACKAGE	CLOTH	20		1
75163-020-20	20 pack Alcohol Hand Wipes-Fresh	4 mL in 1 PATCH	CLOTH	4		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75163-020	20 PACK ALCOHOL HAND WIPES-FRESH CLOTH [ZHUJI JIANHE PAPER CO., LTD]	1	Legacy NDC, 2 package rows	20200924_affdc266-8f3b-d25e-e053-2995a90a2da5.zip

Products#

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

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

20 pack Alcohol Hand Wipes-Fresh
LAVENDER OIL
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75163-020	75163-020-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LAVENDER OIL	ZBP1YXW0H8	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
affdc266-8f3a-d25e-e053-2995a90a2da5			affdc266-8f3b-d25e-e053-2995a90a2da5	2020-09-23	Warnings	Exact identifier spl id: affdc266-8f3a-d25e-e053-2995a90a2da5 spl set id: affdc266-8f3b-d25e-e053-2995a90a2da5

Reported adverse events (FAERS/openFDA)#

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