FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
SCAASIS ORIGINALS INC
Effective date
2020-05-26
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:14:38

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

To decrease bacteria on the skin when water, soap & towel are not available - Recommended for repeated use.

Dosage and administration

Apply enough product to wet hands. Rub hands together until dry. Supervise children in use of this product

Storage and handling

Do not store above 105 *F (40 *C). May discolor some fabric or wood surfaces

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin when water, soap & towel are not available - Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only

Flammable - Keep away from fire or flame

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of contact with eyes , rinse thoroughly with water. Do not use on broken or irritated skin

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop and last more than 72 hours

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

Directions

DOSAGE & ADMINISTRATION SECTION

Apply enough product to wet hands. Rub hands together until dry. Supervise children in use of this product

Other Information

STORAGE AND HANDLING SECTION

  • Do not store above 105 *F (40 *C).
  • May discolor some fabric or wood surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Carbomer, Aminomethyl Propanol, Fragrance(Parfum), Aloe Barbadensis Leaf Extract, Glycerin

Questions?

OTC - QUESTIONS SECTION

+ 732-775-7474

PRINCIPAL DISPLAY PANEL - 250 ML Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HAND
SANITIZER

KILLS
99.9%
GERMS

CONTAINS
70% ETHYL
ALCOHOL

TOPICAL SOLUTION

WITH ALOE &
VITAMIN E

Kills More Than 99.9% of Germs
Leaves Hands Feeling Soft

8.5 FL OZ (250 ML)

PRINCIPAL DISPLAY PANEL - 250 ML Bottle Label
PRINCIPAL DISPLAY PANEL - 250 ML Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN4
581662ethanol 0.7 ML/ML Topical GelSCD4
581662ethanol 70 % Topical GelSY4
581662ethyl alcohol 70 % Topical GelSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75624-123-012023-01-30C16284748780-1f386c64a-11ce-0266-e053-dadaa90a7c1aHAND SANITIZER
75624-123-022023-01-30C16284748780-1f386c64a-11ce-0266-e053-dadaa90a7c1aHAND SANITIZER
75624-123-032023-01-30C16284748780-1f386c64a-11ce-0266-e053-dadaa90a7c1aHAND SANITIZER
75624-123-042023-01-30C16284748780-1f386c64a-11ce-0266-e053-dadaa90a7c1aHAND SANITIZER
75624-123-052023-01-30C16284748780-1f386c64a-11ce-0266-e053-dadaa90a7c1aHAND SANITIZER
75624-123-062023-01-30C16284748780-1f386c64a-11ce-0266-e053-dadaa90a7c1aHAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75624-123-01HAND SANITIZER415 mL in 1 BOTTLE, DISPENSINGGEL4154
75624-123-02HAND SANITIZER200 mL in 1 BOTTLE, DISPENSINGGEL2004
75624-123-03HAND SANITIZER110 mL in 1 BOTTLE, DISPENSINGGEL1104
75624-123-04HAND SANITIZER250 mL in 1 BOTTLE, PUMPGEL2504
75624-123-05HAND SANITIZER120 mL in 1 BOTTLE, DISPENSINGGEL1204
75624-123-06HAND SANITIZER500 mL in 1 BOTTLE, PUMPGEL5004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75624-123HAND SANITIZER (ALCOHOL) GEL [SCAASIS ORIGINALS INC]4Legacy NDC, 6 package rows20200527_0d37f818-b908-43ec-9a96-46c248d10e1d.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75624-12375624-123-01, 75624-123-02, 75624-123-03, 75624-123-04, 75624-123-05, 75624-123-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
ALOE VERA LEAFZY81Z83H0XIACT

Source Document#

Source XML · Source PDF

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
a5d96a2d-f4fd-4990-b599-50648ec531f00d37f818-b908-43ec-9a96-46c248d10e1d2020-05-26WarningsExact identifier
spl id: a5d96a2d-f4fd-4990-b599-50648ec531f0
spl set id: 0d37f818-b908-43ec-9a96-46c248d10e1d

Reported adverse events (FAERS/openFDA)#

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