FDA.reportPublic FDA data

ALCOHOL WIPES

Manufacturer
Pnr Group, LLC | FuYang YangYang Health Technology Co. Ltd
Effective date
2020-08-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:54

Label at a glance#

ProductALCOHOL WIPES
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Wipes hands thoroughly, let skin dry and discard. Keep out of children. Children under 6 years use only under adult supervision. Not recommended for infants.

Storage and handling

Do not store above 105℉. May discolor some fabrics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Alcohol Wet Wipes

Use

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin that may cause disease.

Usage:

Open lid---Pull out wipe from center---Close lid to retain moisture---Do no flush.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire and flame.

Do not use

OTC - DO NOT USE SECTION

  • Do not use in or near the eyes. In case of contact with eyes, flush thoroughly with water. Use wipes only on unbroken, intact skin. If you have sensitive skin or certain allergies, check the list of ingredients on the label before using wipes. Do not ingest.

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

OTC - STOP USE SECTION

Stop use and ask a doctor. if skin irritation or redness develops.

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

Wipes hands thoroughly, let skin dry and discard.

Keep out of children. Children under 6 years use only under adult supervision.

Not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

Do not store above 105℉. May discolor some fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe vera, Citrus Scent.

SPL UNCLASSIFIED SECTION

ALCOHOL WIPES

SANITIZING WET WIPES

Kills 99.9% of Bacteria*

LEMON SCENT

75% ALCOHOL

80 WIPES

CLEAN & MOISTURIZES

Great for use at Home, work and on th GO!

NO TRICLOSAN & PARABENS NO WASH CHEMICALS

SAFE & GENTLE ON SKIN

DO NOT FLUSH WIPES!

Effective at eliminating 99.99% of many common/harmful germs and becteria in as little as 15 seconds.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80 Wipes NDC: 11749-080-80

80 wipes label80 wipes label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11749-080-802022-01-28C16284748780-1d6a99b39-7914-a426-e053-dadaa90af4c211749-080-80 ALCOHOL WIPES /ALCOHOL WIPES FuYang YangYang Health Technology Co. Ltd .

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11749-080-80ALCOHOL WIPES5.5 g in 1 PATCHCLOTH5.51
11749-080-80ALCOHOL WIPES80 in 1 PAILCLOTH801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11749-080ALCOHOL WIPES (SANITIZING WET WIPES) CLOTH [PNR GROUP, LLC]1Legacy NDC, 2 package rows20200817_acf93048-498d-1b6f-e053-2a95a90a1a57.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11749-08011749-080-80

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
acf93048-498e-1b6f-e053-2a95a90a1a57acf93048-498d-1b6f-e053-2a95a90a1a572020-08-16WarningsExact identifier
spl id: acf93048-498e-1b6f-e053-2a95a90a1a57
spl set id: acf93048-498d-1b6f-e053-2a95a90a1a57

Reported adverse events (FAERS/openFDA)#

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