KUNDAL PURE and SAFE SANITIZING WIPE (ETHANOL)

Manufacturer
THESKINFACTORY Co., Ltd. | Sauber Co.,Ltd.
Effective date
2020-10-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:30:58

Label at a glance#

ProductKUNDAL PURE and SAFE SANITIZING WIPE (ETHANOL)
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

alcohol

INACTIVE INGREDIENT SECTION

Water
Glycerin
Camellia Sinensis Leaf Extract

calendula officinalis flower extract

OTC - PURPOSE SECTION

hand sanitizing tissue to help reduce bacteria on the skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

plae enough product on hands to cover all surfaces, rub hands together until dry

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 product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse 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.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74773-0029-12022-07-29C16284748780-1e4f33bdf-a648-d8a0-e053-dadaa90a6e4eaeeaeecf-d2a7-0934-e053-2a95a90a1a41

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74773-0029-1KUNDAL PURE and SAFE SANITIZING WIPE (ETHANOL)5 g in 1 POUCHLIQUID52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74773-0029KUNDAL PURE AND SAFE SANITIZING WIPE (ETHANOL) (ALCOHOL) LIQUID [THESKINFACTORY CO., LTD.]2Legacy NDC, 1 package rows20201004_aeeaeecf-d2a7-0934-e053-2a95a90a1a41.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
74773-002974773-0029-1

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
b0d2158c-da1e-1e7b-e053-2a95a90a004daeeaeecf-d2a7-0934-e053-2a95a90a1a412020-10-04WarningsExact identifier
spl id: b0d2158c-da1e-1e7b-e053-2a95a90a004d
spl set id: aeeaeecf-d2a7-0934-e053-2a95a90a1a41

Reported adverse events (FAERS/openFDA)#

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