FDA.reportPublic FDA data

ALLPURE HAND SANITIZER

Manufacturer
YESILILGAZ KOZMETIK KIMYA INSAAT OTOMOTIV VE GIDA SANAYI TICARET LIMITED SIRKETI
Effective date
2020-07-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:22:14

Label at a glance#

ProductALLPURE HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Place enough product on hands to cover all surfaces.. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer 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

Do not use

  • in children less than 2 months of age
  • on open skin wounds

When using this products 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

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

  • Place enough product on hands to cover all surfaces.. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

Store above 15·30C (59·86F)

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Glycerin, Purified Water, Rosmarinus Officinalis Extract, Triethanolamine

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78575-002-012022-01-28C16284748780-1d6a99b39-c540-a426-e053-dadaa90af4c2549422db-8693-41f6-8312-7fb2ef40b0b7
78575-002-022022-01-28C16284748780-1d6a99b39-c540-a426-e053-dadaa90af4c2549422db-8693-41f6-8312-7fb2ef40b0b7
78575-002-032022-01-28C16284748780-1d6a99b39-c540-a426-e053-dadaa90af4c2549422db-8693-41f6-8312-7fb2ef40b0b7
78575-002-042022-01-28C16284748780-1d6a99b39-c540-a426-e053-dadaa90af4c2549422db-8693-41f6-8312-7fb2ef40b0b7
78575-002-052022-01-28C16284748780-1d6a99b39-c540-a426-e053-dadaa90af4c2549422db-8693-41f6-8312-7fb2ef40b0b7
78575-002-062022-01-28C16284748780-1d6a99b39-c540-a426-e053-dadaa90af4c2549422db-8693-41f6-8312-7fb2ef40b0b7
78575-002-072022-01-28C16284748780-1d6a99b39-c540-a426-e053-dadaa90af4c2549422db-8693-41f6-8312-7fb2ef40b0b7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78575-002-01ALLPURE HAND SANITIZER30 mL in 1 BOTTLE, PLASTICGEL301
78575-002-02ALLPURE HAND SANITIZER50 mL in 1 BOTTLE, PLASTICGEL501
78575-002-03ALLPURE HAND SANITIZER100 mL in 1 BOTTLE, PLASTICGEL1001
78575-002-04ALLPURE HAND SANITIZER250 mL in 1 BOTTLE, PLASTICGEL2501
78575-002-05ALLPURE HAND SANITIZER500 mL in 1 BOTTLE, PLASTICGEL5001
78575-002-06ALLPURE HAND SANITIZER1000 mL in 1 BOTTLE, PLASTICGEL10001
78575-002-07ALLPURE HAND SANITIZER5000 mL in 1 BOTTLE, PLASTICGEL50001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78575-002ALLPURE HAND SANITIZER (ALCOHOL) GEL [YESILILGAZ KOZMETIK KIMYA INSAAT OTOMOTIV VE GIDA SANAYI TICARET LIMITED SIRKETI]1Legacy NDC, 7 package rows20200723_549422db-8693-41f6-8312-7fb2ef40b0b7.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78575-00278575-002-01, 78575-002-02, 78575-002-03, 78575-002-04, 78575-002-05, 78575-002-06, 78575-002-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)4Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
ROSEMARYIJ67X351P9IACT

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
9472c36d-7580-4e1e-8735-641bf8a5d30b549422db-8693-41f6-8312-7fb2ef40b0b72020-07-08WarningsExact identifier
spl id: 9472c36d-7580-4e1e-8735-641bf8a5d30b
spl set id: 549422db-8693-41f6-8312-7fb2ef40b0b7

Reported adverse events (FAERS/openFDA)#

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