PPE Company Care Instant Hand Sanitiser

Manufacturer
PPE Company Care Ltd
Effective date
2020-11-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:33:19

Label at a glance#

ProductPPE Company Care Instant Hand Sanitiser
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

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

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75% v/

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

Hand sanitiser 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

In children less than 2 months of age.
On open skin 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 - STOP USE 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 Centre right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

SPL UNCLASSIFIED SECTION

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

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Phenoxyethanol, Aminomethyl Propanol.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottleBottle2Bottle2

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
80856-000-012022-01-28C16284748780-1d6a99b39-9905-a426-e053-dadaa90af4c2PPE Company Care Instant Hand Sanitiser

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80856-000-01PPE Company Care Instant Hand Sanitiser60 mL in 1 BOTTLEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80856-000PPE COMPANY CARE INSTANT HAND SANITISER (ALCOHOL) GEL [PPE COMPANY CARE LTD]1Legacy NDC, 1 package rows20201110_b3b0c8cd-992b-2acc-e053-2995a90a5cd8.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80856-00080856-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
b3b0df66-e648-3eb2-e053-2995a90a91d9b3b0c8cd-992b-2acc-e053-2995a90a5cd82020-11-09WarningsExact identifier
spl id: b3b0df66-e648-3eb2-e053-2995a90a91d9
spl set id: b3b0c8cd-992b-2acc-e053-2995a90a5cd8

Reported adverse events (FAERS/openFDA)#

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