FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Sunflora Inc | Inspec Solutions LLC
Effective date
2020-12-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:00:40

Label at a glance#

ProductHand Sanitizer Sunmed
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin.

Dosage and administration

Place enough product on your palm to thoroughly cover your hands • Rub hands together briskly until dry.

Label contents#

Full prescribing information#

Active ingredient                       Purpose

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%                       Antiseptic                         

Warnings For external use only. Flammable: Do not use while smoking or near heat or flame.

WARNINGS SECTION

When using this product• Keep out of eyes. Rinse with water to remove.
Stop use and ask doctor if irritation or rash appears and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Polson Control Center lmmediately.

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on your palm to thoroughly cover your hands • Rub hands together briskly until dry.

Other infonnation

OTHER SAFETY INFORMATION

store below 110 0  (43°C )

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aminomethyl Propanol, Carbomer, Fragrance, Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Water Hemp Extract.

Questions?

OTC - QUESTIONS SECTION

727-235-0120

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73240-01473240-014-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)4Q93RCW27EIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
b6fac1c7-78fd-7228-e053-2995a90a4b7740da4fda-cde7-4063-bc05-ac1a61e50f722020-12-21WarningsExact identifier
spl id: b6fac1c7-78fd-7228-e053-2995a90a4b77
spl set id: 40da4fda-cde7-4063-bc05-ac1a61e50f72

Reported adverse events (FAERS/openFDA)#

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