Hemptuary Hawaii Hand Sanitizer 16 oz

Manufacturer
Aloha Green Holdings Inc.
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:46:37

Label at a glance#

ProductHemptuary Hawaii Hand Sanitizer 16 oz
Active ingredientISOPROPYL ALCOHOL
Label structure8 sections

Indications and uses

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

Dosage and administration

Apply product onto hands, spread thoroughly, cover all surfaces, and rub until dry. Supervise children children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

Apply product onto hands, spread thoroughly, cover all surfaces, and rub until dry.

Supervise children children under 6 years of age when using this product to avoid swallowing.

Warnings

WARNINGS SECTION

Flamable. Keep away from heat or flame. For external use only.

Do not ingest. If swallowed, get medical help or contact a Poison Center right away. Keep out of reach of children.

Do not use for children less than 2 months of age or on open wounds.

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyle alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Do not use for children less than 2 month sof age or on open wounds.

Front of Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hemptuary Hawaii Hand Santizer

Isopopoyl Alcohol Antiseptic 75% topical, non-sterile solution

16oz (473ml)

Front Label of PackageFront Label of Package

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73999-001-012024-01-30C16284748780-11030e365-6b44-111a-e063-dadaa90a10e2a18f0710-9b21-ed5e-e053-2995a90abcd3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73999-001-01Hemptuary Hawaii Hand Sanitizer 16 oz473 mL in 1 BOTTLE, PUMPGEL4732

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73999-001HEMPTUARY HAWAII HAND SANITIZER 16 OZ (ISOPROPYL ALCOHOL) GEL [ALOHA GREEN HOLDINGS INC.]2Legacy NDC, 1 package rows20220113_a18f0710-9b21-ed5e-e053-2995a90abcd3.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73999-00173999-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
d571b4c4-7e88-7012-e053-2a95a90a8ef5a18f0710-9b21-ed5e-e053-2995a90abcd32022-01-13WarningsExact identifier
spl id: d571b4c4-7e88-7012-e053-2a95a90a8ef5
spl set id: a18f0710-9b21-ed5e-e053-2995a90abcd3

Reported adverse events (FAERS/openFDA)#

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