FDA.reportPublic FDA data

Oomph Antiseptic Instant Hand Sanitizer Gel

Manufacturer
Pascoe's Pty. Ltd.
Effective date
2021-10-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:31:58

Label at a glance#

ProductOomph Antiseptic Instant Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 80%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • for hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

  • in the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

SPL UNCLASSIFIED SECTION

  • Store below 86°F (30°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 alkyl acrylate crosspolymer, denatonium benzoate, glycerin, hydrogen peroxide, triethanolamine, water.

Package Labeling: 2.3ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2.3Label2.3

Package Labeling: 50ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label50Label50

Package Labeling: 250ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label250Label250

Package Labeling: 450ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label450Label450

Package Labeling: 500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label500Label500

Package Labeling: 1L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label1000Label1000

Package Labeling: 5L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5000Label5000

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79319-00079319-000-00, 79319-000-01, 79319-000-08, 79319-000-15, 79319-000-16, 79319-000-33, 79319-000-66

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
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
ceb59225-d095-296b-e053-2995a90a541cae7d0854-c8aa-1db3-e053-2995a90a47b72021-10-19WarningsExact identifier
spl id: ceb59225-d095-296b-e053-2995a90a541c
spl set id: ae7d0854-c8aa-1db3-e053-2995a90a47b7

Reported adverse events (FAERS/openFDA)#

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