Hand Sanitizer

Manufacturer
Luminary Distilling, LLC
Effective date
2020-03-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:04:16

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Directions * 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#

Warnings

WARNINGS SECTION

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

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Active ingredient[s] Purpose

Alcohol 76.95% Antiseptic

Do not use

OTC - DO NOT USE SECTION

Do not use

* in children less than 2 months of age

* on open skin wounds

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor 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

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients purified water USP (21.025%), isopropyl alcohol (4.95%), glycerin (1.875%), hydrogen peroxide (0.15%)

Other information

OTHER SAFETY INFORMATION

Other information

* Store between 15-30C (59-86F)

* Avoid freezing and excessive heat above 40C (104F)

Use[s]

INDICATIONS & USAGE SECTION

Use[s]

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

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

* 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.

Purpose

OTC - PURPOSE SECTION

Purpose

Antiseptic

Luminary Distilling Liquid Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Liquid Hand SanitizerLiquid Hand Sanitizer
Liquid Hand Sanitizer

Non-Sterile Solution

Alcohol Antiseptic 76.95%

Topical Solution

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73888-101-01Hand Sanitizer18927.059 mL in 1 BOTTLE, PLASTICLIQUID18927.0592
73888-101-02Hand Sanitizer750 mL in 1 BOTTLE, GLASSLIQUID7502
73888-101-03Hand Sanitizer118.294 mL in 1 BOTTLE, SPRAYLIQUID118.2942

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73888-101HAND SANITIZER (ETHYL ALCOHOL) LIQUID [LUMINARY DISTILLING, LLC]2Legacy NDC, 3 package rows20200330_a1769504-3632-97df-e053-2995a90a8aa1.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
73888-10173888-101-02, 73888-101-03, 73888-101-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
a1f67afc-b335-240d-e053-2995a90ad837a1769504-3632-97df-e053-2995a90a8aa12020-03-28WarningsExact identifier
spl id: a1f67afc-b335-240d-e053-2995a90ad837
spl set id: a1769504-3632-97df-e053-2995a90a8aa1

Reported adverse events (FAERS/openFDA)#

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