Ohana Mahaalo Hand Gel PA

Manufacturer
Fragrancy Inc.
Effective date
2020-11-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:07:20

Label at a glance#

ProductOhana Mahaalo Hand Gel PA
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Wet hand thoroughly with product and allow to dry without wiping Place enough product in the palm of your hands to thoroughly cover you hands. Rub hands together briskly until product is completely absorbed and hands are dry. Inactive Ingredients:

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80 %

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

Warnings

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

When using this product do not use in or near the eyes.

In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

INDICATIONS & USAGE SECTION

Wet hand thoroughly with product and allow to dry without wiping

DOSAGE & ADMINISTRATION SECTION

Place enough product in the palm of your hands to thoroughly cover you hands. Rub hands together briskly until product is completely absorbed and hands are dry.

Inactive Ingredients:

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

water, glycerin, cabomer, PEG-60 hydrogenated castor oil, fragrance, tetrahydrooxypropyl ethylenediamine, 1,2-hexandiol, betaine, cyprylyl glycol, alpha-isomethyl ionone, butylene glycol, tocoperhol, methylpropanediol, camellia sinensis leaf extract, sodium hyaluronate, soluble collagen, ethylhexylglyerin, butylated hydroxytoulene

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ohana Mahaalo Hand Gel PA.jpgOhana Mahaalo Hand Gel PA.jpg

Products#

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DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81074-000381074-0003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
c57b71cd-1568-d9b8-e053-2a95a90a64b9b3f5cc64-7298-fa3a-e053-2a95a90a1a4f2021-06-23WarningsExact identifier
spl set id: b3f5cc64-7298-fa3a-e053-2a95a90a1a4f

Reported adverse events (FAERS/openFDA)#

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