FDA.reportPublic FDA data

Ollie Hand Sanitizer

Manufacturer
F.P. Aromatics Singapore Pte Ltd
Effective date
2023-04-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:54:41

Label at a glance#

ProductOllie Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

To sanitize hand when soap and water are not available.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To sanitize hand when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Keep away from fire or flame.

Do not use

  • on open wounds
  • on children less than 4 months of age.

When using this product, keep out of eyes, ears, mouth.
Stop use and ask a doctor if irritation or rash occurs.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Direction

DOSAGE & ADMINISTRATION SECTION

  • Spray on hands and rub them together gently
  • Supervise children under 6 years of age in the use of this product

Other information

SPL UNCLASSIFIED SECTION

Store between 15° - 30°C (59° - 86°F)

Inactive ingredient

INACTIVE INGREDIENT SECTION

Aloe vera, Orange oil, Peppermint oil, Tea tree oil, Water

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN3
1041849ethanol 0.7 ML/ML Topical SpraySCD3
1041849ethanol 70 % Topical SpraySY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81634-001-012024-07-30C16284748780-1f386c649-fe4f-0266-e053-dadaa90a7c1acfb33479-2d53-4925-9fdc-acf2e6e514ab
81634-001-012024-01-30C16284748780-1f386c649-fe4f-0266-e053-dadaa90a7c1acfb33479-2d53-4925-9fdc-acf2e6e514ab
81634-001-012023-04-11C16284748780-1f386c649-fe4f-0266-e053-dadaa90a7c1acfb33479-2d53-4925-9fdc-acf2e6e514ab
81634-001-012023-01-30C16284748780-1f386c649-fe4f-0266-e053-dadaa90a7c1acfb33479-2d53-4925-9fdc-acf2e6e514ab

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81634-001-01Ollie Hand Sanitizer30 mL in 1 BOTTLE, GLASSLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81634-001OLLIE HAND SANITIZER (ALCOHOL) LIQUID [F.P. AROMATICS SINGAPORE PTE LTD]3Legacy NDC, 1 package rows20230412_cfb33479-2d53-4925-9fdc-acf2e6e514ab.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
81634-00181634-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
ORANGE OILAKN3KSD11BIACT
PEPPERMINT OILAV092KU4JHIACT
TEA TREE OILVIF565UC2GIACT
ALCOHOL3K9958V90MACTIB

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
f90effbe-3915-8f70-e053-6294a90aedfdcfb33479-2d53-4925-9fdc-acf2e6e514ab2023-04-11WarningsExact identifier
spl id: f90effbe-3915-8f70-e053-6294a90aedfd
spl set id: cfb33479-2d53-4925-9fdc-acf2e6e514ab

Reported adverse events (FAERS/openFDA)#

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