FDA.reportPublic FDA data

70% SafetyPlus Hand Sanitizer 32oz

Manufacturer
SafetyPlus, Inc. | Orange Lab, Inc. | Orange Lab, Inc
Effective date
2022-02-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:55:44

Label at a glance#

Product70% SafetyPlus Hand Sanitizer 32oz
Active ingredientALCOHOL
Label structure14 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

Stop use and ask a doctor if skin irritation develops.

OTC - ASK DOCTOR SECTION

Ask a doctorAsk a doctor

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Purpose : Antiseptic

OTC - PURPOSE SECTION

PurposePurpose

Questions ?

OTC - QUESTIONS SECTION

questionsquestions

Stop use and ask a doctor if skin irritation develops.

OTC - STOP USE SECTION

Stop useStop use

When using this product section

OTC - WHEN USING SECTION

When using this productWhen using this product

Directions section

INSTRUCTIONS FOR USE SECTION

DirectionsDirections

Other safety information

Other safety informationOther safety information

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredientInactive ingredient

Warnings section

warningswarnings

Dosage & Administration section

DosageDosage

Indications & Usage section

Indications and usageIndications and usage

Package front label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front panelFront panel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80174-109-012024-01-30C16284748780-1d6a99b39-5f42-a426-e053-dadaa90af4c2SafetyPlus Hand Sanitizer with Aloe 70% 32oz
80174-109-012022-08-08C16284748780-1d6a99b39-5f42-a426-e053-dadaa90af4c2SafetyPlus Hand Sanitizer with Aloe 70% 32oz
80174-109-012022-01-28C16284748780-1d6a99b39-5f42-a426-e053-dadaa90af4c2SafetyPlus Hand Sanitizer with Aloe 70% 32oz

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80174-10970% SAFETYPLUS HAND SANITIZER 32OZ (ETHYL ALCOHOL) GEL [SAFETYPLUS, INC.]4Legacy NDC20220810_ad40ee47-3810-9fa4-e053-2995a90a6b8e.zip

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
80174-10980174-109-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
PANTHENOLWV9CM0O67ZIACT
CARBOMER COPOLYMER TYPE A71DD5V995LIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
4f10aaab-4854-44ad-e063-6394a90a274cad40ee47-3810-9fa4-e053-2995a90a6b8e2026-04-09WarningsExact identifier
spl set id: ad40ee47-3810-9fa4-e053-2995a90a6b8e

Reported adverse events (FAERS/openFDA)#

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