OTC Medication Information: ILOJE CLEAN AND SAFE HAND SANITIZER

ILOJE CLEAN AND SAFE HAND SANITIZER- alcohol gel
KONAD CO LTD

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.

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antimicrobial

Inactive Ingredients

Water, Glycerin, Butylene Glycol, Aloe Barbadensis Leaf Extract, 1,2-Hexanediol, Camell ia Sinensis Leaf Extract, Sophora Flavesc ens Root Extract, Carbomer, Triethanolamine, Fragrance

A hand cleaner

‚ÄčA hand cleaner that is easy to carry and can use without water directly

How to Use

Put a suitable amount on your hand and rub it well to dry.

Cautions in Use

2) In case of hypersensitivity symptoms such as rash, erythema, itching, edema, etc.

3) In case of skin irritation symptoms.

5) Be careful not to get into the eye. If it does, wash it well with clean water and consult a doctor or pharmacist.

Cautions in Use

8) Store out of the reach of children and go to the hospital immediately if swallowed by children.

Cautions in Use

1) Around the eyes and ears, within the mouth, extensive body parts and damaged skin. (It can cause stimulation)

4) For external use only. (do not use internally)

Warnings

For external use only. Flammable. Keep away from heat or flame.

Cautions in Use

6) Be careful not to inhale steam when used extensively or for long periods of time.

7) Keep away from fire.

9) After use, completely close the product with a lid to prevent it from drying or entering foreign substances.

Package Label

100ml NDC: 74740-601-01 Label
(click image for full-size original)

300ml NDC: 74740-601-02 Label
(click image for full-size original)
500ml NDC: 74740-601-03 Label
(click image for full-size original)
ILOJE CLEAN AND SAFE HAND SANITIZER
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:74740-601
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 70 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
ALOE VERA LEAF 0.088 mL in 100 mL
SOPHORA FLAVESCENS ROOT 0.087 mL in 100 mL
1,2-HEXANEDIOL 0.004 mL in 100 mL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE 0.35 mL in 100 mL
WATER 27.903 mL in 100 mL
BUTYLENE GLYCOL 1.011 mL in 100 mL
TROLAMINE 0.35 mL in 100 mL
GLYCERIN 0.12 mL in 100 mL
GREEN TEA LEAF 0.087 mL in 100 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:74740-601-01 100 mL in 1 BOTTLE None
2 NDC:74740-601-02 300 mL in 1 BOTTLE, PUMP None
3 NDC:74740-601-03 500 mL in 1 BOTTLE, PUMP None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 04/19/2020
Labeler — KONAD CO LTD (688329887)
Registrant — KONAD CO LTD (688329887)
Establishment
Name Address ID/FEI Operations
KONAD CO LTD 688329887 manufacture (74740-601)

Revised: 01/2022 KONAD CO LTD

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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