Hand Sanitizer

Manufacturer
Blackland Distillery
Effective date
2020-06-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:19:00

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

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

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands until dry. Supervise children under 6 years of age who are using this product to avoid swallowing.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Purpose

OTC - PURPOSE SECTION

Alcohol 80% v/v ……… Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warning

WARNINGS SECTION

For external use only – hands

Flammable

Keep away from fire and flame

Do not use

OTC - DO NOT USE SECTION

  • on children less than 2 months of age.
  • on open skin wounds.

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash occurs. These may be a sign of a serious condition.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands until dry.

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

Other Information

SPL UNCLASSIFIED SECTION

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

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe, Fragrance, Glycerin, Hydrogen Peroxide, Reverse Osmosis Water

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


Hand Sanitizer
Juniper scent
8 fl oz (237 ml)

PRINCIPAL DISPLAY PANEL Hand Sanitizer Juniper scent 8 fl oz (237 ml)PRINCIPAL DISPLAY PANEL Hand Sanitizer Juniper scent 8 fl oz (237 ml)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78816-001-012022-01-28C16284748780-1d6a99b39-75ce-a426-e053-dadaa90af4c2Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78816-001-01Hand Sanitizer237 mL in 1 BOTTLELIQUID2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78816-001HAND SANITIZER (ALCOHOL) LIQUID [BLACKLAND DISTILLERY]1Legacy NDC, 1 package rows20200626_0f130b0f-fb87-49e7-9cf7-a779f5408a8d.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78816-00178816-001-01

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
ca0a9656-9ba6-476a-bd08-a47655f79eac0f130b0f-fb87-49e7-9cf7-a779f5408a8d2020-06-16WarningsExact identifier
spl id: ca0a9656-9ba6-476a-bd08-a47655f79eac
spl set id: 0f130b0f-fb87-49e7-9cf7-a779f5408a8d

Reported adverse events (FAERS/openFDA)#

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