Hand Sanitizer

Manufacturer
Great health companion Medical device technology group co., LTD
Effective date
2020-06-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:24

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Open packet. Lightly squeeze the packet into the palm of your hand with enough product to cover both of hands. Rub hands together, spread product over the backs of each hand, and in between each finger. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store between 59-86 ℉ (15-30℃). Avoid freezing. Avoid excessive heat above 104 ℉ (40 ℃).

Label contents#

Full prescribing information#

ACTIVE INGREDIENT(S)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75% v/v.

labellabel

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For use when antibacterial soap and water are not available.
Recommended for repeated use.
Hand sanitizer to help reduce illness causing bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Do not use on open skin wounds.
When using this product, keep out or AWAY from eyes, ears, nose and mouth. In case of unwanted, rinse thoroughly with water.
Stop use and seek help form a licensed doctor or medical professional if rash or irritation occurs as these may be signs of a serious condition or illness.
Keep out of reach of children. Do not use on children less than 2 months of age. Children under 6 years of age should be supervised when using this product to avoid swallowing.
Do not swallow or ingest. If swallowed, seek medical help and contact a Poison Control Center immediately.
Flammable. Keep away from sources of heat or fire.

May be harmful to some fabrics, wood finishes and plastics.

Do not use

OTC - DO NOT USE SECTION

on children less than 2 months of age.

on open skin wounds.e

WHEN USING

OTC - WHEN USING SECTION

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

STOP USE

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

These maybe signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

Directions

DOSAGE & ADMINISTRATION SECTION

Open packet. Lightly squeeze the packet into the palm of your hand with enough product to cover both of hands. Rub hands together, spread product over the backs of each hand, and in between each finger.
Children under 6 years of age should be supervised when using this product.

Other Information

STORAGE AND HANDLING SECTION

Store between 59-86 ℉ (15-30℃).

Avoid freezing. Avoid excessive heat above 104 ℉ (40 ℃).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Glycerin, Aloe barbadensis leaf extract, Carbomer, Aminomethyl Propanol, Hydrogenated castor oil, Tocopheryl acetate

PACKAGE LABEL- PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package lablepackage lable

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78765-001-012023-01-30C16284748780-1f386c649-c23d-0266-e053-dadaa90a7c1ahand sanitizer 75% alcohol based

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78765-001-01Hand Sanitizer3 mL in 1 PACKETGEL31

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78765-001HAND SANITIZER (ALCOHOL) GEL [GREAT HEALTH COMPANION MEDICAL DEVICE TECHNOLOGY GROUP CO., LTD]1Legacy NDC, 1 package rows20200620_a7395fe8-3e9c-f169-e053-2a95a90a1642.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78765-00178765-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
a7395fe8-3e9d-f169-e053-2a95a90a1642a7395fe8-3e9c-f169-e053-2a95a90a16422020-06-06WarningsExact identifier
spl id: a7395fe8-3e9d-f169-e053-2a95a90a1642
spl set id: a7395fe8-3e9c-f169-e053-2a95a90a1642

Reported adverse events (FAERS/openFDA)#

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