Global Care Hand Sanitizer, Ethyl Alcohol

Manufacturer
TARGET PRICE INC
Effective date
2020-05-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:28:29

Label at a glance#

ProductGlobal Care Hand Sanitizer, Ethyl Alcohol
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

hand santizer to help reduce bacteria on the skin.

Dosage and administration

wet hands thoroughly with product and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using.   

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 64%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

hand santizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops.

Keep out of reach of childen.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and rub into skin until dry.
  • Children under 6 years of age should be supervised by an adult when using.   

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene glycol, Glycerine, Triethanolamine, Unopol

Packag Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72146-020-012025-02-10C16284748780-10191ceaa-6dac-198a-e063-dbdaa90aec3eGlobal Care Hand Sanitizer, Ethyl Alcohol
72146-020-012023-07-28C16284748780-10191ceaa-6dac-198a-e063-dbdaa90aec3eGlobal Care Hand Sanitizer, Ethyl Alcohol

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
72146-02072146-020-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
0c5bf826-e506-6a56-e063-6394a90a866ca6ce3834-d2e8-7ac7-e053-2995a90a5d412025-02-10WarningsExact identifier
spl set id: a6ce3834-d2e8-7ac7-e053-2995a90a5d41

Reported adverse events (FAERS/openFDA)#

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