Hand Sanitizer

Manufacturer
Oingo Products LLC
Effective date
2020-08-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:25:22

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

For additional information, see Safety Data Sheets (SDS) | For emergency medical information in USA and Canada, call 1-888-255-3924 | Store between 15- 30C (59-86F) | Avoid freexing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 65% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only, Flammable, keep away from fire or flame, heat, sparks, and sources of static discharge

Do not use

OTC - DO NOT USE SECTION

  • In eyes | on children less than 2 months of age | on open skin wounds

When using this product

OTC - WHEN USING SECTION

If in eyes, rinse promptly and thoroughly with water | Discontinue use if irritation and redness develops

Stop use and ask a doctor

OTC - STOP USE SECTION

If skin irritation or redness occurs or persists for more than 72 hours.

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 on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

For additional information, see Safety Data
Sheets (SDS) | For emergency medical information in USA and
Canada, call 1-888-255-3924 | Store between 15-
30C (59-86F) | Avoid freexing and excessive heat above 40C
(104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water (aqua), propylene glycol,
dimethicone PEG-7 Isostearate, acrylates/ C10-30 Alkyl
Acrylate Crosspolymer, aminomethylpropanediol, tocopherol
acetate, aloe barbadensis leaf juice

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59 mL NDC: 79436-102-0159 mL NDC: 79436-102-0159 mL NDC: 79436-102-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
902515ethanol 65 % Topical SprayPSN1
902515ethanol 0.65 ML/ML Topical SpraySCD1
902515ethanol 65 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79436-102-012022-01-28C16284748780-1d6a99b39-e0b1-a426-e053-dadaa90af4c2ad4075b3-7b42-6759-e053-2a95a90aed30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79436-102-01Hand Sanitizer40000 mL in 1 BOTTLE, SPRAYSPRAY400001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79436-102HAND SANITIZER (ALCOHOL) SPRAY [OINGO PRODUCTS LLC]1Legacy NDC, 1 package rows20200821_ad4075b3-7b42-6759-e053-2a95a90aed30.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79436-10279436-102-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
LAVENDER OILZBP1YXW0H8IACT
GLYCERINPDC6A3C0OXIACT

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
ad408102-be06-ca51-e053-2a95a90a5808ad4075b3-7b42-6759-e053-2a95a90aed302020-08-19WarningsExact identifier
spl id: ad408102-be06-ca51-e053-2a95a90a5808
spl set id: ad4075b3-7b42-6759-e053-2a95a90aed30

Reported adverse events (FAERS/openFDA)#

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