Hand Sanitizer

Manufacturer
Supply Direct LLC
Effective date
2020-06-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:58

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

■ Apply a dime sized amount to hands. Rub hands together until dry ■ Supervise children under 6 years of age when using this product to avoid swallowing

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from flame or heat.

Do not use

OTC - DO NOT USE SECTION

■ On children less than 2 months of age ■ On open skin wounds

When using this product

OTC - WHEN USING SECTION

■ Do not use in or near eyes. ■ In case of contact, immediately rinse eyes throughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation or rash appears ■ conditions persist for more than 72 hours ■ if redness is present

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If accident or swallowed, contact a doctor or poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Apply a dime sized amount to hands. Rub hands together until dry ■ Supervise children under 6 years of age when using this product to avoid swallowing

Other information

SPL UNCLASSIFIED SECTION

Store between 15º-30ºC (59-86ºF). ■ May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis leaf juice, Glycerin, Tocopheryl Acetate (Vitamin E), Triethanolamine, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer

Questions

OTC - QUESTIONS SECTION

Tel: 332-210-9092 (Mon-Fri 9am-5pm EST)

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77886-001-02Hand Sanitizer60 mL in 1 BOTTLE, PLASTICGEL601
77886-001-08Hand Sanitizer236 mL in 1 BOTTLE, PLASTICGEL2361
77886-001-16Hand Sanitizer500 mL in 1 BOTTLE, PLASTICGEL5001
77886-001-33Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77886-001HAND SANITIZER (ALCOHOL) GEL [SUPPLY DIRECT LLC]1Legacy NDC, 4 package rows20200604_a731c607-e517-c83f-e053-2995a90ab892.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
77886-00177886-001-33, 77886-001-08, 77886-001-16, 77886-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
a731dfd1-bdf6-c4f3-e053-2995a90a4511a731c607-e517-c83f-e053-2995a90ab8922020-06-03WarningsExact identifier
spl id: a731dfd1-bdf6-c4f3-e053-2995a90a4511
spl set id: a731c607-e517-c83f-e053-2995a90ab892

Reported adverse events (FAERS/openFDA)#

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