Hand Sanitizer

Manufacturer
Oingo Products LLC
Effective date
2020-08-18
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

Apply product onto hands, spread thoroughly and rub dry | Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Other Information 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

Ethyl Alcohol 62.5% v/v…………………..……... Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

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

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

Apply product onto hands, spread thoroughly and

rub dry | Supervise children under 6 years of age when using

this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

Other Information 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

Purpose

OTC - PURPOSE SECTION

​Antiseptic, Hand Sanitizer

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1893 mL NDC: 79436-101-061893 mL NDC: 79436-101-06946 mL NDC: 79436-101-05946 mL NDC: 79436-101-05236.5 mL NDC: 79436-101-03236.5 mL NDC: 79436-101-03236.5 mL NDC: 79436-101-03

473 mL NDC: 79436-101-04473 mL NDC: 79436-101-04473 mL NDC: 79436-101-04

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79436-101-03Hand Sanitizer30000 mL in 1 BOTTLE, PUMPGEL300001
79436-101-04Hand Sanitizer10000 mL in 1 BOTTLE, PLASTICGEL100001
79436-101-05Hand Sanitizer10000 mL in 1 BOTTLE, PUMPGEL100001
79436-101-06Hand Sanitizer10000 mL in 1 BOTTLE, PUMPGEL100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79436-101HAND SANITIZER (ALCOHOL) GEL [OINGO PRODUCTS LLC]1Legacy NDC, 4 package rows20200821_ad2c4ce6-0931-3cec-e053-2995a90a6d82.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79436-10179436-101-04, 79436-101-03, 79436-101-05, 79436-101-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
ad2c1d6f-4b81-b1ad-e053-2a95a90a9c26ad2c4ce6-0931-3cec-e053-2995a90a6d822020-08-18WarningsExact identifier
spl id: ad2c1d6f-4b81-b1ad-e053-2a95a90a9c26
spl set id: ad2c4ce6-0931-3cec-e053-2995a90a6d82

Reported adverse events (FAERS/openFDA)#

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