FDA.reportPublic FDA data

Hudson Scientific Hand Sanitizer

Manufacturer
Hudson Scientific LLC
Effective date
2020-06-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:27:13

Label at a glance#

ProductHudson Scientific Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Cover hands thoroughly with product and allow to dry without wiping. Supervise children in the use of this product.

Storage and handling

Store at 20 to 25 degrees C (68 to 77 degrees F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 72.34%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Usage

INDICATIONS & USAGE SECTION

To decrease bacteria on skin.

Recommended for repeated use.

Warnings

WARNINGS SECTION

Flamable: keep away from fire or flame.

For external use only.

Do not get in eyes.  In case of contact, rince eyes thoroughly with water.

Stop use and consult a doctor if irritation and redness develops, and condition persists for 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 for use

DOSAGE & ADMINISTRATION SECTION

Cover hands thoroughly with product and allow to dry without wiping.

Supervise children in the use of this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Aloe, Barbadenisi Leaf Juice, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl acetate, Acrylates/C10-30 Alkyle Acrelate, Crosspolyme Aminomethyle Propenol

Storage

STORAGE AND HANDLING SECTION

Store at 20 to 25 degrees C (68 to 77 degrees F)

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front Label: Hand Sanitizer Label- FrontHand Sanitizer Label- Front

Back Label: Hand Sanitizer Label- BackHand Sanitizer Label- Back

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70914-04170914-041-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
AloeV5VD430YW9IACT
GOSSYPIUM BARBADENSE LEAF251DUP3OSNIACT
CAPRYLYL GLYCOL00YIU5438UIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
(C10-C30)ALKYL METHACRYLATE ESTERXH2FQZ38D8IACT
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
2f2c722e-234b-40c0-be0d-d47e1ecaa341461ca131-adcf-4dc9-b9f1-9530381dccf72021-11-30WarningsExact identifier
spl set id: 461ca131-adcf-4dc9-b9f1-9530381dccf7

Reported adverse events (FAERS/openFDA)#

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