Premium Gel Alcohol Hand Sanitizer

Manufacturer
Dade Paper & Bag, Llc
Effective date
2020-07-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:23:51

Label at a glance#

ProductPremium Gel Alcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

​To decrease bacteria on the skin that could cause disease - Recommended for repeated use.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping For children under 6, use only under adult supervision ■ Not recommended for infants.

Storage and handling

Do not store above 105°F ■ May discolor some fabrics Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

​To decrease bacteria on the skin that could cause disease - Recommended for repeated use.

WARNINGS:

WARNINGS SECTION

For external use only: Hands.

FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.

When using this product ■ Keep out of eyes. In case of contact with eyes, flush thoroughly with water ■ Avoid contact with broken skin ■ Do not inhale or ingest ■ Stop use and ask a doctor if: irritation and redness develop or 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:

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping
For children under 6, use only under adult supervision ■ Not recommended for infants.

Other information:

STORAGE AND HANDLING SECTION

Do not store above 105°F ■ May discolor some fabrics
Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized Water, Aloe Vera Gel (Aloe Barbadensis Leaf Juice), Carbomer, Triethanolamine, Vitamin E (Tocopheryl Acetate).

SPL UNCLASSIFIED SECTION

Distributed by Imperial Dade

Manufactured for Imperial Dade

www.imperialdade.com

255 Route 1 & 9

Jersey City, NJ 07306.

MADE IN USA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Premium1Premium1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71907-200-222022-01-28C16284748780-1d6a99b39-5de2-a426-e053-dadaa90af4c2PREMIUM GEL ALCOHOL HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71907-200-22Premium Gel Alcohol Hand Sanitizer3.78 L in 1 BOTTLEGEL3.781
71907-200-22Premium Gel Alcohol Hand Sanitizer2 in 1 CASEGEL21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71907-200PREMIUM GEL ALCOHOL HAND SANITIZER (ETHYL ALCOHOL) GEL [DADE PAPER & BAG, LLC]1Legacy NDC, 2 package rows20200806_9d1b926e-ba75-4d28-838e-ec40b1fee2d5.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
71907-20071907-200-22

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
d10b7f90-b278-4ddf-81c4-4df4e4e852109d1b926e-ba75-4d28-838e-ec40b1fee2d52020-07-30WarningsExact identifier
spl id: d10b7f90-b278-4ddf-81c4-4df4e4e85210
spl set id: 9d1b926e-ba75-4d28-838e-ec40b1fee2d5

Reported adverse events (FAERS/openFDA)#

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