HAND SANITIZER GEL - 70% ETHYL ALCOHOL

Manufacturer
Sunshine Tape Products LLC
Effective date
2020-05-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:18

Label at a glance#

ProductHAND SANITIZER 70 PERCENT
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Helps reduce bacteria on the skin.

Dosage and administration

Dispense enough product onto hands and rub together quickly until dry. Children under 6 years of age, use only under adult supervision.

Storage and handling

Store below 110°F (43°C). May cause discoloration to fabrics and/or surfaces.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70%

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USES

INDICATIONS & USAGE SECTION

Helps reduce bacteria on the skin.

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame. When using this product avoid contact with eyes. In case of contact flush thoroughly with water. Avoid contact with open skin. Stop use and ask doctor if irritation or rash develops.

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 immediately.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Dispense enough product onto hands and rub together quickly until dry. Children under 6 years of age, use only under adult supervision.

Additional Information:

STORAGE AND HANDLING SECTION

Store below 110°F (43°C). May cause discoloration to fabrics and/or surfaces.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Purified Water, Propylene Glycol, Glycerin, Carbomer, Triethanolamine, Tocopherol Acetate, Coconut Oil, Aloe Vera Gel, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_2oz Drug Facts Template01b LBL_2oz Drug Facts Template

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74598-112-11HAND SANITIZER70 PERCENT3785 mL in 1 JUGGEL37851
74598-112-12HAND SANITIZER70 PERCENT59 mL in 1 BOTTLEGEL591
74598-112-14HAND SANITIZER70 PERCENT118 mL in 1 BOTTLEGEL1181
74598-112-16HAND SANITIZER70 PERCENT476 mL in 1 BOTTLEGEL4761
74598-112-18HAND SANITIZER70 PERCENT237 mL in 1 BOTTLEGEL2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74598-112HAND SANITIZER 70 PERCENT (ETHYL ALCOHOL) GEL [SUNSHINE TAPE PRODUCTS LLC]1Legacy NDC, 5 package rows20200509_66f8f027-3855-4054-bc38-431a4d7d5fca.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74598-11274598-112-18, 74598-112-14, 74598-112-16, 74598-112-11, 74598-112-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
bbb10001-79bd-4352-ae4b-c9e0ca809ab166f8f027-3855-4054-bc38-431a4d7d5fca2020-05-08WarningsExact identifier
spl id: bbb10001-79bd-4352-ae4b-c9e0ca809ab1
spl set id: 66f8f027-3855-4054-bc38-431a4d7d5fca

Reported adverse events (FAERS/openFDA)#

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