JANITEX ALCOHOL WET WIPES 70%

Manufacturer
Pacific Health Systems Inc.
Effective date
2020-08-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:25:30

Label at a glance#

ProductJANITEX ALCOHOL WET WIPES 70%
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• For hand sanitizing to decrease bacteria and germs on skin. • Apply topically to the skin to help prevent cross contamination. • Dries in seconds.

Dosage and administration

• Lift the tab on the top of the lid to open. • Open moisture seal film package before use. • Pull out first wipe through the dispensing center of the canister. Next sheets pops up automatically • Close the lid to retain moisture. • Wipe dean with this product. Let air dry

Storage and handling

• Store at room temperature 15-30°C (59-86°F). • Lot No. Manufacture date and expiration date can be found on package.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 67%

Purpose

OTC - PURPOSE SECTION

Antiseptic

INACTIVE INGREDIENT SECTION

Inactive Ingredients   Isopropyl Alcohol 3%, Aqua, Glycerin, Parfum

Uses

INDICATIONS & USAGE SECTION

• For hand sanitizing to decrease bacteria and germs on skin.

• Apply topically to the skin to help prevent cross contamination.

• Dries in seconds.

Warnings

WARNINGS SECTION

• For external use only. Harmful if swallowed.

• Do not use as baby wipes.

• Do not flush down the toilet. Highly flammable.

• Keep away from fire or flame. Do not use in or contact the eyes. Avoid contact with open or exposed wounds.

Do not Use

• Do not use as baby wipes.

• Do not flush down the toilet.

• Highly flammable. Keep away from fire or flame.

• Do not eat or drink when handling.

• Avoid contact with open or exposed

When Using

Keep out of eyes, ears, and mouth.

In case of contact with eyes, rinse eyes thoroughly with water

Stop Use

Stop use if too much skin irritation and sensitivity develops or increases

KEEP OUT OF REACH OF CHILDREN

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

• Lift the tab on the top of the lid to open.

• Open moisture seal film package before use.

• Pull out first wipe through the dispensing center of the canister. Next sheets pops up automatically

• Close the lid to retain moisture.

• Wipe dean with this product. Let air dry

Other Informations

STORAGE AND HANDLING SECTION

• Store at room temperature 15-30°C (59-86°F).

• Lot No. Manufacture date and expiration date can be found on package.

SPL UNCLASSIFIED SECTION

+ ANTIBACTERIAL + ANTI - FUNGAL

BLEACH FREE

Dry Wipes Size: 15*18 cm 5,9 x 7,1 inch

Suitable for sensitive skin

Kills 99.9% Bacteria & Germs

ALCOHOL WIPES

Alcohol Concentration

Efficient Sterilization

Non-Woven Skin

Moisturizes and Does Not Dry

Distributed by Pacific Health Inc. 19 Commerce

Road Unit E Fairfield, NJ 07004

info@janitexus.com www.janitexus.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79519-030-012022-01-28C16284748780-1d6a99b39-c816-a426-e053-dadaa90af4c2JANITEX 70% ALCOHOL WET WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79519-030-01JANITEX ALCOHOL WET WIPES 70%3 mL in 1 PACKAGECLOTH31
79519-030-01JANITEX ALCOHOL WET WIPES 70%40 in 1 PACKETCLOTH401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79519-030JANITEX ALCOHOL WET WIPES 70% (ETHYL ALCOHOL) CLOTH [PACIFIC HEALTH SYSTEMS INC.]1Legacy NDC, 2 package rows20200822_d4da44f7-2f61-4105-a64f-60bbc342c141.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79519-03079519-030-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
754a1992-8d75-43a2-a41f-299119178303d4da44f7-2f61-4105-a64f-60bbc342c1412020-08-19WarningsExact identifier
spl id: 754a1992-8d75-43a2-a41f-299119178303
spl set id: d4da44f7-2f61-4105-a64f-60bbc342c141

Reported adverse events (FAERS/openFDA)#

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