FDA.reportPublic FDA data

MEDOVE Instant Hand Sanitiser

Manufacturer
YIWU MINGYAN COSMETICS CO., LTD.
Effective date
2020-05-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:30:14

Label at a glance#

ProductMEDOVE Instant Hand Sanitiser
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Dosage and administration

Pump a small amount into palm of hands Rub thoroughly over all surface of both hands Rub hands together briskly untill dry

Storage and handling

Do not store above 105F May discolor wood or fabrics Harmful to wood finishes or plastics

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NA

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to help decrease bacteria on the skin

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame when using this product

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of contact with eyes, flush eyes with water.

OTC - STOP USE SECTION

Do not inhale or ingest

Stop use and ask a doctor if irritation or redness develops, or if condition persists for 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

  • Pump a small amount into palm of hands
  • Rub thoroughly over all surface of both hands
  • Rub hands together briskly untill dry

Other information

STORAGE AND HANDLING SECTION

  • Do not store above 105F
  • May discolor wood or fabrics
  • Harmful to wood finishes or plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, carbomer, triethanolamine, Essence

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75168-00175168-001-01, 75168-001-02, 75168-001-03, 75168-001-04, 75168-001-05, 75168-001-06, 75168-001-07, 75168-001-08, 75168-001-09, 75168-001-10, 75168-001-11, 75168-001-12, 75168-001-13, 75168-001-14, 75168-001-15, 75168-001-16, 75168-001-17, 75168-001-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER 934Z135WT9208IACT
TRIETHANOLAMINE SULFATEMV1V89M17OIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

Source Document#

Source XML · Source PDF

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
ae4cd12c-0f6c-1809-e053-2a95a90adeed58c4cbe3-3931-41b8-8ade-17eee19e1aaf2020-09-01WarningsExact identifier
spl set id: 58c4cbe3-3931-41b8-8ade-17eee19e1aaf

Reported adverse events (FAERS/openFDA)#

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