MVP SANITIZER TISSUE

Manufacturer
KONAD CO., LTD
Effective date
2020-07-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:22:59

Label at a glance#

ProductMVP SANITIZER TISSUE
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

How to Use

DOSAGE & ADMINISTRATION SECTION

Open cover, pull needed number of sheets, reseal after each use.

Cautions in Use

WARNINGS SECTION

1) For external use only.

2) THESE WIPES DO NOT REPLACE WIPES USED FOR MEDICAL PROCEDURES. THESE WIPES ARE MEANT FOR GENERAL CLEANING.

3) Keep in a dry place away from fire.

Cautions in Use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

4) Keep this product out of reach of children.

Cautions in Use

OTC - ASK DOCTOR SECTION

5) If swallowed, get immediate medical help, or contact the nearest Poison Control Center.

6) Do not use in, or contact the eyes. If contact occurs flush immediately with water.

7) Discontinue use if irritation and/or redness occur. If the condition persists for more than 72 hours, consult a physician immediately.

Cautions in Use

INDICATIONS & USAGE SECTION

8) Storage and handling;

A) Avoid storing under direct sunlight, or expose to continuous high heat.

B) Do not discard in the toilet as it may cause clogging.

C) Please close the lid after dispensing to maintain purity. Alcohol by nature evaporates quickly

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Poloxamer 184, Cocamidopropyl Betaine, PEG-7 Glyceryl Cocoate, Butylene Glycol, Sodium Chloride, Aloe Barbadensis Leaf Extract, Thymus Vulgaris (Thyme) Extract, So phora Flavescens Root Extract, Sodium Hyaluronate, Cetylpyridinium Chloride, Hydroxyaceto phenone, PEG-60 Hydrogenated Castor Oil, Citricacid, Menthol, 1,2-Hexanediol, Fragrance

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

400g NDC: 74740-602-01 Label400g NDC: 74740-602-01 Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74740-602-012023-08-28C16284748780-1d6a99b39-7647-a426-e053-dadaa90af4c274740-602
74740-602-012022-01-28C16284748780-1d6a99b39-7647-a426-e053-dadaa90af4c274740-602

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74740-60274740-602-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
0406b66d-f73b-db85-e063-6394a90a19fda9131d24-7d52-4e7f-e053-2a95a90ad6d22023-08-28WarningsExact identifier
spl set id: a9131d24-7d52-4e7f-e053-2a95a90ad6d2

Reported adverse events (FAERS/openFDA)#

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