Creamol Hand Sanitizer Wipe

Manufacturer
LABER KIMYA AR-GE SANAYI TICARET - LEVENT KAHRIMAN
Effective date
2020-09-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:28:33

Label at a glance#

ProductCreamol Hand Sanitizer Wipe
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wipe hands and dischard.

Storage and handling

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

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethanol alcohol 80%. (w/w) Purpose: Antimicrobial

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available. Wipe hands; discard.

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

OTC - DO NOT USE SECTION

Do not use,

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

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 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

Wipe hands and dischard.

Other information

STORAGE AND HANDLING SECTION

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

INACTIVE INGREDIENT SECTION

glycerin, Hypericum perforatum, Melaleuca alternifolia, water, parfum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 77892-0009-1 innerNDC: 77892-0009-1 innerNDC: 77892-0009-1 outerNDC: 77892-0009-1 outerNDC: 77892-0009-1 innerNDC: 77892-0009-1 inner

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2361646ethanol 80 % Medicated PadPSN2
2361646ethanol 0.8 ML/ML Medicated PadSCD2
2361646ethanol 80 % Medicated WipesSY2
2361646ethyl alcohol 80 % Topical ClothSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77892-0009-12021-07-23C16284748780-1c7ccaba7-271e-fd44-e053-dadaa90aa01bCREAMOL HAND SANITIZING WIPE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77892-0009-1Creamol Hand Sanitizer Wipe4 g in 1 POUCHSWAB42

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77892-0009CREAMOL HAND SANITIZER WIPE (ALCOHOL) SWAB [LABER KIMYA AR-GE SANAYI TICARET - LEVENT KAHRIMAN]2Legacy NDC, 1 package rows20200907_ae6314f8-cec4-54d6-e053-2995a90a6210.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
77892-000977892-0009-1

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
aeb42668-ea4d-8920-e053-2a95a90abfd2ae6314f8-cec4-54d6-e053-2995a90a62102020-09-07WarningsExact identifier
spl id: aeb42668-ea4d-8920-e053-2a95a90abfd2
spl set id: ae6314f8-cec4-54d6-e053-2995a90a6210

Reported adverse events (FAERS/openFDA)#

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