Sani Gel

Manufacturer
Omega Industrial Supply | QuestSpecialty Corporation
Effective date
2024-12-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:41:17

Label at a glance#

ProductSani Gel
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Handwash to help decrease bacterial on the skin. Recommended for repeated use.

Dosage and administration

Place a palmful ( 5 grams) of product in one hand,. Spread on both hands and rub into the skin until dry (approximately 1 to 2 minutes). Place a smaller amount (2.5 grams) into one hand, spread over both hands to wrist and rub into the skin until dry (approximately 30 seconds). Will air dry in 15 seconds.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 60%..........Antiseptic

purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Handwash to help decrease bacterial on the skin.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

  • Flammable. Keep away from fire or flame.
  • For external use only.

do not use

OTC - DO NOT USE SECTION

  • In the eyes

When Using

OTC - WHEN USING SECTION

  • Do not use in or near the eyes.
  • If contact occurs, flush eyes with water for 15 minutes. Consult physician if irritation persists.
  • If swallowed, seek medical assistance or consult a poison control center immediately.

Stop Use

OTC - STOP USE SECTION

  • Stop use and ask a doctor if: Irritation develops. If condition persists for more than 72 hours consult a doctor.
  • Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

Directions for Use

DOSAGE & ADMINISTRATION SECTION

  • Place a palmful ( 5 grams) of product in one hand,.
  • Spread on both hands and rub into the skin until dry (approximately 1 to 2 minutes).
  • Place a smaller amount (2.5 grams) into one hand, spread over both hands to wrist and rub into the skin until dry (approximately 30 seconds).
  • Will air dry in 15 seconds.

OTHER SAFETY INFORMATION

  • Store below 95 o F.
  • Close spout to avoid evaporation.

INACTIVE INGREDIENT SECTION

Water, triethanolamine, fragrance, acrylic polymer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sani Gel galSani Gel galSani Gel 4ozSani Gel 4oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68642-693-01Sani Gel118 mL in 1 BOTTLE, PLASTICLIQUID1182
68642-693-03Sani Gel3785 mL in 1 BOTTLE, PLASTICLIQUID37852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68642-693SANI GEL LIQUID [OMEGA INDUSTRIAL SUPPLY]2Current NDC, Legacy NDC, 2 package rows20241209_bda9bd59-9825-27ba-e053-2a95a90a3002.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
68642-69368642-693-01, 68642-693-03

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
CARBOMER 9404Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
Sani GelSANI GELOmega Industrial Supplybda9bd59-9825-27ba-e053-2a95a90a30022024-12-08WarningsExact identifier
ndc (package): 68642-693-03
ndc (package): 68642-693-01
ndc (product): 68642-693
ndc11 (package): 68642069303
ndc11 (package): 68642069301
spl id: 28c54ac2-c524-7eb5-e063-6394a90aa52d
spl set id: bda9bd59-9825-27ba-e053-2a95a90a3002

Reported adverse events (FAERS/openFDA)#

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