Klenlii Sanii Wipes
FDA Label NDC 78016-105

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Klenlii Company for the product Klenlii Sanii Wipes (NDC 78016-105). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

ETHYL ALCOHOL 75%

Purpose

ANTISEPTIC

Uses

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

Warnings

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

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

Directions

  • 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

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

Inactive Ingredients

water (aqua), glycerin

* Please review the disclaimer below.