Mellow 59ml hand sanitizer original

Manufacturer
Mission Y,Inc. | Shenzhen Lantern Science Co.,Ltd.
Effective date
2020-04-28
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
full-release
Hydrated at
2026-05-31 23:08:40

Label at a glance#

ProductMellow 59ml hand sanitizer original
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Wet hands thoroughly with product and rub until dry without wiping For children under 6, use only under adult supervision. Not recommended for infants. When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Do not inhale or ingest. Avoid contact with broken skin. Do not store above 105F. May discolor some fabrics. Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Drug Facts

DESCRIPTION SECTION

75580-001-01.jpg75580-001-01.jpg

Medicical Ingredient

OTC - ACTIVE INGREDIENT SECTION

Medicical Ingredient Purpose

Ethyl Alcohol 75%(V/V) Antiseptic

Features

OTC - PURPOSE SECTION

To decrease bacteria on the skin that could cause disease.

Recommended for repeated use.

Use anywhere without water.

DOSAGE & ADMINISTRATION SECTION

Recommended for repeated use.

use anywhere without water.

Warning

WARNINGS SECTION

For external use only-hands.

Flammable,keep away from heat and flame.

Discontinue if skin becomes irritated and ask a doctor.

Keep out of reach of children. In case of accidental ingestion,seek professional assistance or contact a Poison Control Center immediately.

WARNINGS AND PRECAUTIONS SECTION

For external use only.

Flammable, keep away from heat and flame.

OTC - STOP USE SECTION

Discontinue if skin becomes irritated and ask a doctor .

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a poson control center immediately.

Non-Medicinal

INACTIVE INGREDIENT SECTION

Water, Glycerin,Propylene Glycol,Carbomer,,Aminomethyl propanol,Parfum.

Directions

INDICATIONS & USAGE SECTION

Wet hands thoroughly with product and rub until dry without wiping

For children under 6, use only under adult supervision.

Not recommended for infants.

OTC - DO NOT USE SECTION

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Do not inhale or ingest.

Avoid contact with broken skin.

Other information

CLEANING, DISINFECTING, AND STERILIZATION INSTRUCTIONS

Do not store above 105F.

May discolor some fabrics.

Harmful to wood finishes and plastics.

When using this product

OTC - WHEN USING SECTION

keep out of eyes,In case of contact with eyes,flush thoroughly with water

Do not inhale or ingest

Avoid contact with broken skin.

other information

OTHER SAFETY INFORMATION

Do not store above 105℉

May discolor some fabrics.

Harmful to wood finishes and plastics。

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75580-001-01.jpg75580-001-01.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN11
1305100ethanol 0.75 ML/ML Topical GelSCD11
1305100ethanol 75 % Topical GelSY11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75580-005-012022-01-28C16284748780-1d6a99b39-569b-a426-e053-dadaa90af4c2Mellow 59ml hand sanitizer original

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75580-005-01Mellow 59ml hand sanitizer original59 mL in 1 BOTTLE, PLASTICLIQUID5911

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75580-005MELLOW 59ML HAND SANITIZER ORIGINAL (ALCOHOL) LIQUID [MISSION Y,INC.]11Legacy NDC, 1 package rows20200429_a4664226-d2fd-6744-e053-2995a90ae366.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75580-00575580-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
a4664226-d2fe-6744-e053-2995a90ae366a4664226-d2fd-6744-e053-2995a90ae3662020-04-28WarningsExact identifier
spl id: a4664226-d2fe-6744-e053-2995a90ae366
spl set id: a4664226-d2fd-6744-e053-2995a90ae366

Reported adverse events (FAERS/openFDA)#

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