ALLPURE HAND SANITIZER SANITIZING WIPE

Manufacturer
CERCI KOZMETIK VE OTEL EKIPMANLARI PAZARLAMA IC VE DIS TICARET LIMITED SIRKETI
Effective date
2023-10-31
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:02:17

Label at a glance#

ProductALLPURE HAND SANITIZER SANITIZING WIPE
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Antiseptic wipe to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame. Keep out of reach of children.

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 productkeep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

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

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry without wiping.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

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

Glycerin, Butylene Glycol, Water, Lanolin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Label 2Label 2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489307ethanol 70 % Medicated PadPSN4
1489307ethanol 0.7 ML/ML Medicated PadSCD4
1489307ethanol 70 % Medicated PadSY4
1489307ethanol 70 % Medicated WipesSY4
1489307ethyl alcohol 70 % ClothSY4

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80176-001-01ALLPURE HAND SANITIZER SANITIZING WIPE1 in 1 PACKETCLOTH14
80176-001-01ALLPURE HAND SANITIZER SANITIZING WIPE5 mL in 1 POUCHCLOTH54
80176-001-02ALLPURE HAND SANITIZER SANITIZING WIPE5 mL in 1 POUCHCLOTH54
80176-001-02ALLPURE HAND SANITIZER SANITIZING WIPE10 in 1 PACKETCLOTH104
80176-001-03ALLPURE HAND SANITIZER SANITIZING WIPE5 mL in 1 POUCHCLOTH54
80176-001-03ALLPURE HAND SANITIZER SANITIZING WIPE50 in 1 PACKETCLOTH504
80176-001-04ALLPURE HAND SANITIZER SANITIZING WIPE5 mL in 1 POUCHCLOTH54
80176-001-04ALLPURE HAND SANITIZER SANITIZING WIPE72 in 1 PACKETCLOTH724
80176-001-05ALLPURE HAND SANITIZER SANITIZING WIPE120 in 1 PACKETCLOTH1204
80176-001-05ALLPURE HAND SANITIZER SANITIZING WIPE5 mL in 1 POUCHCLOTH54
80176-001-06ALLPURE HAND SANITIZER SANITIZING WIPE200 in 1 PACKETCLOTH2004
80176-001-06ALLPURE HAND SANITIZER SANITIZING WIPE5 mL in 1 POUCHCLOTH54

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80176-001ALLPURE HAND SANITIZER SANITIZING WIPE (ALCOHOL) CLOTH [CERCI KOZMETIK VE OTEL EKIPMANLARI PAZARLAMA IC VE DIS TICARET LIMITED SIRKETI]4Legacy NDC, 12 package rows20231116_eaf57fdb-d4e0-4893-90e3-0c532c921698.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
80176-00180176-001-01, 80176-001-02, 80176-001-03, 80176-001-04, 80176-001-05, 80176-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
09032c0b-a099-2601-e063-6294a90a2d34eaf57fdb-d4e0-4893-90e3-0c532c9216982023-10-31WarningsExact identifier
spl id: 09032c0b-a099-2601-e063-6294a90a2d34
spl set id: eaf57fdb-d4e0-4893-90e3-0c532c921698

Reported adverse events (FAERS/openFDA)#

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