FDA.reportPublic FDA data

Bittol Alcohol Wipes

Manufacturer
Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi
Effective date
2023-12-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:17:40

Label at a glance#

ProductBittol Alcohol Wipes
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

For hand and skin sanitizing. When water, soap & towel are not available. Recommended for repeated use.

Dosage and administration

Children under 6 years of age use only under adult supervision. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222) Not recommended for infants.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand and skin sanitizing.
  • When water, soap & towel are not available.
  • Recommended for repeated use.

WARNINGS

WARNINGS SECTION

  • For external use only.
  • Flammable, keep away from fire or flame.

When Using This Product:

OTC - WHEN USING SECTION

  • Do not use in or near the eyes. In case of eye contact, rinse eyes 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. 

Stop use and ask a doctor:

OTC - STOP USE SECTION

If skin irritation or redness develops.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Children under 6 years of age use only under adult supervision. Keep out of reach of children.
  • If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
  • Not recommended for infants.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children under 6 years of age use only under adult supervision.

Other Information:

SPL UNCLASSIFIED SECTION

  • Store below 110°F (43°C)
  • May discolor certain fabrics or surfaces.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aqua/ Water, Glycerin, Propylene Glycol, Parfum/ Fragrance, Sodium PCA, Disodium EDTA.

Package Labeling:40 Count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:80 Count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Package Labeling:100 Count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

Package Labeling:120 Count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle4Bottle4

Package Labeling:150 Count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle5Bottle5

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
78564-00478564-004-01, 78564-004-02, 78564-004-03, 78564-004-04, 78564-004-05

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM PYRROLIDONE CARBOXYLATE469OTG57A2IACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
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
19c37dc3-80b3-5b99-e063-6294a90adf3c07a47fd5-ac48-4ff9-8a16-0a4cb15e3c3d2024-05-31WarningsExact identifier
spl set id: 07a47fd5-ac48-4ff9-8a16-0a4cb15e3c3d

Reported adverse events (FAERS/openFDA)#

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