FDA.reportPublic FDA data

Alcohol Wipes

Manufacturer
Shaoxing Elite Bio-Tech Co.,Ltd.
Effective date
2023-11-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:02:42

Label at a glance#

ProductAlcohol Wipes
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Open the lid, tear open packet, remove wipe. Wet hands thoroughly with product and let hands air dry. Throw used wipe in trash. Do not flush.

Storage and handling

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on skin.

Warnings

WARNINGS SECTION

For external use only. Flammable: Keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

In children less than 2 months of age.

On open skin wounds.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes and mouth. If in eyes，flush thoroughly with water.

OTC - STOP USE SECTION

Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Open the lid, tear open packet, remove wipe.

Wet hands thoroughly with product and let hands air dry.

Throw used wipe in trash.

Do not flush.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30 °C (59-86 °F).

Avoid freezing and excessive heat above 40 °C (104 °F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC:81079-002-01

1010NDC:81079-002-02

2020NDC:81079-002-03

4040NDC:81079-002-04

6060NDC:81079-002-05

8080NDC:81079-002-06

100100

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN2
1307051ethanol 0.75 ML/ML Medicated PadSCD2
1307051ethanol 75 % Hand Sanitizer WipesSY2
1307051ethyl alcohol 75 % Topical ClothSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81079-002-01Alcohol Wipes38 mL in 1 BAGCLOTH382
81079-002-02Alcohol Wipes76 mL in 1 BAGCLOTH762
81079-002-03Alcohol Wipes153 mL in 1 BAGCLOTH1532
81079-002-04Alcohol Wipes230 mL in 1 BAGCLOTH2302
81079-002-05Alcohol Wipes307 mL in 1 BAGCLOTH3072
81079-002-06Alcohol Wipes384 mL in 1 BAGCLOTH3842

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81079-002ALCOHOL WIPES (ALCOHOL) CLOTH [SHAOXING ELITE BIO-TECH CO.,LTD.]2Current NDC, Legacy NDC, 6 package rows20231123_b42c2735-ead2-4db9-e053-2a95a90a229f.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81079-00281079-002-01, 81079-002-02, 81079-002-03, 81079-002-04, 81079-002-05, 81079-002-06

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
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Alcohol WipesALCOHOLShaoxing Elite Bio-Tech Co.,Ltd.b42c2735-ead2-4db9-e053-2a95a90a229f2023-11-22WarningsExact identifier
ndc (package): 81079-002-02
ndc (package): 81079-002-04
ndc (package): 81079-002-06
ndc (package): 81079-002-03
ndc (package): 81079-002-01
ndc (package): 81079-002-05
ndc (product): 81079-002
ndc11 (package): 81079000205
ndc11 (package): 81079000206
ndc11 (package): 81079000201
ndc11 (package): 81079000203
ndc11 (package): 81079000202
ndc11 (package): 81079000204
spl id: 0ab86da8-eb13-46d1-e063-6294a90a4fe7
spl set id: b42c2735-ead2-4db9-e053-2a95a90a229f

Reported adverse events (FAERS/openFDA)#

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