Hand Sanitizer-Antibacterial Hand Sanitizer

Manufacturer
Consumer Health and Safety Products
Effective date
2020-05-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:25

Label at a glance#

ProductHand Sanitizer-Antibacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Place enough product in your palm to throoughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin that could cause disease.

Warnings

WARNINGS SECTION

Flammable, Keep away from fire or flame.

For External Use only.

When Using this product.

OTC - WHEN USING SECTION

do not use in or near the eyes, in case of contact, rinse throughly with water.

Stop Using this product.

OTC - STOP USE SECTION

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 Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in your palm to throoughly cover your hands. Rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

OTHER SAFETY INFORMATION

  • Store below 110°F (43°C)

Ingredients

INACTIVE INGREDIENT SECTION

Alcohol, Water, Acrylates(C-10/30 Alkyl Acylate) Crosspolymer, Aloe Vera, Triethanolamine.

Package Label - Principal Disaplay Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60ml Label60ml Label236 ml Label236 ml Label

60 mL NDC: 77968-070-02

236 mL NDC: 77968-070-01

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
77968-070-012022-01-28C16284748780-1d6a99b39-579e-a426-e053-dadaa90af4c2Hand Sanitizer - Antibacterial Hand Sanitizer
77968-070-022022-01-28C16284748780-1d6a99b39-579e-a426-e053-dadaa90af4c2Hand Sanitizer - Antibacterial Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77968-070-01Hand Sanitizer-Antibacterial Hand Sanitizer236 mL in 1 BOTTLEGEL2361
77968-070-02Hand Sanitizer-Antibacterial Hand Sanitizer60 mL in 1 BOTTLEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77968-070HAND SANITIZER-ANTIBACTERIAL HAND SANITIZER (HAND SANITIZER GEL) GEL [CONSUMER HEALTH AND SAFETY PRODUCTS]1Legacy NDC, 2 package rows20200518_a5c6d6be-5b15-a625-e053-2995a90af5a9.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77968-07077968-070-01, 77968-070-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
a5c6d6be-5b16-a625-e053-2995a90af5a9a5c6d6be-5b15-a625-e053-2995a90af5a92020-05-16WarningsExact identifier
spl id: a5c6d6be-5b16-a625-e053-2995a90af5a9
spl set id: a5c6d6be-5b15-a625-e053-2995a90af5a9

Reported adverse events (FAERS/openFDA)#

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