MEDCILLARY Hand Sanitizer

Manufacturer: MLS
Effective date: 2020-06-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:25:57

Label at a glance#

ProductMEDCILLARY Hand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

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

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

DOSAGE & ADMINISTRATION SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

on children less than 2 months of age

on open wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

INDICATIONS & USAGE SECTION

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

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)

Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Methylpropanediol, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract, Butylene Glycol, Carbomer, Triethanolamine, 1,2-Hexanediol, Fragrance

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80ml NDC: 73984-331-01 Label

500ml NDC: 73984-331-02 Label

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

MEDCILLARY Hand Sanitizer
ALCOHOL
HYALURONATE SODIUM
1,2-HEXANEDIOL
ORANGE PEEL
WATER
ALOE VERA LEAF
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
METHYLPROPANEDIOL
BUTYLENE GLYCOL
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73984-331	73984-331-01, 73984-331-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
HYALURONATE SODIUM	YSE9PPT4TH	IACT
1,2-HEXANEDIOL	TR046Y3K1G	IACT
ORANGE PEEL	TI9T76XD44	IACT
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
METHYLPROPANEDIOL	N8F53B3R4R	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
TROLAMINE	9O3K93S3TK	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
b9380f49-bdab-3f09-e053-2995a90a38e0			a7f9e829-a8f4-d72d-e053-2995a90a01d2	2021-01-18	Warnings	Exact identifier spl set id: a7f9e829-a8f4-d72d-e053-2995a90a01d2

Reported adverse events (FAERS/openFDA)#

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