Kuri Hand Sanitizer: Package Insert and Label Information

KURI HAND SANITIZER- alcohol liquid
Kuri Enterprises

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

DRUG FACTS

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Use

For hand-washing to decrease bacteria on the skin, only when water is not available.

Warnings

-Flammable, Keep away from heat or flame

-For external use only.

When using this product

  • Do not get into eyes
  • If contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

  • Irritation and redness develop

Keep out of reach of children

Directions

  • Wet hands thoroughly with product and allow to dry without wiping

Inactive Ingredients

Water, glycerin, Acrylates/dimethicome copolymer, Methylchloroisothiazolinone, Methylisothiazolinone, Triethanolamine, Aloe Vera Extract

Package Labeling

Label
(click image for full-size original)

KURI HAND SANITIZER
alcohol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:79560-001
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 0.7 mL in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
GLYCERIN
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
TROLAMINE
ALOE VERA LEAF
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:79560-001-01 250 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 06/23/2020
Labeler — Kuri Enterprises (077014675)

Revised: 07/2020 Kuri Enterprises

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2022. All Rights Reserved.