KLENLII SANII WIPES

Manufacturer
Klenlii Company
Effective date
2024-05-09
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:12:20

Label at a glance#

ProductKLENLII SANII WIPES 75 PERCENT
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

DECREASE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE RECOMMENDED FOR REPEATED USE

Dosage and administration

wet and clean hands thoroughly with a wipe and allow to dry for children under 6, ask a doctor before use not recommended for infants

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 75%

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USES

INDICATIONS & USAGE SECTION

  • DECREASE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE
  • RECOMMENDED FOR REPEATED USE

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY: HANDS

Store in a cool, dry place, away from heat and direct sunlight.

When using this product

  • keep out of eyes
  • in case of contact with eyes, flush thoroughly with water
  • avoid contact with broken skin
  • do not inhale or digest

Stop use and ask a doctor if

  • irritation or redness develops
  • condition persists more than 72 hours

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

  • wet and clean hands thoroughly with a wipe and allow to dry
  • for children under 6, ask a doctor before use
  • not recommended for infants

OTHER INFORMATION

OTHER SAFETY INFORMATION

  • may discolor fabrics
  • may be harmful to wood finishes and plastics

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

water (aqua), glycerin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Klenlii_Sanii Wipes_250ct01b LBL_Klenlii_Sanii Wipes_250ct

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78016-105-11KLENLII SANII WIPES75 PERCENT250 in 1 POUCHSOLUTION2505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78016-105KLENLII SANII WIPES 75 PERCENT (ALCOHOL) SOLUTION [KLENLII COMPANY]5Legacy NDC, 1 package rows20240511_1e77bb92-f0ea-442d-baa6-e582b18a8053.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78016-10578016-105-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
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
180c5cd6-b36d-210b-e063-6394a90aed261e77bb92-f0ea-442d-baa6-e582b18a80532024-05-09WarningsExact identifier
spl id: 180c5cd6-b36d-210b-e063-6394a90aed26
spl set id: 1e77bb92-f0ea-442d-baa6-e582b18a8053

Reported adverse events (FAERS/openFDA)#

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