FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Beaming White LLC
Effective date
2022-01-28
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:11:13

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Dispense a small amount onto palm of hand and rub briskly and thoroughly over surfaces of both hands until dry. Children under 6 years of age should be supervised while using this product.

Storage and handling

Store below 110 °F (43 °C) May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to reduce bacterial organisms on the skin.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Dispense a small amount onto palm of hand and rub briskly and thoroughly over surfaces of both hands until dry.
  • Children under 6 years of age should be supervised while using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store below 110 °F (43 °C)
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Acrylates/c10-30 Alkyl Acrylate Crosspolymer, Triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3.75L Label3.75L Label1 GALLON (3.78L) NDC: 75669-0003-99

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75669-0003-22022-01-30C16284748780-1d6a99b39-6091-a426-e053-dadaa90af4c2Koala Hand Sanitizer - Unscented
75669-0003-32022-01-30C16284748780-1d6a99b39-6091-a426-e053-dadaa90af4c2Koala Hand Sanitizer - Unscented
75669-0003-62022-01-30C16284748780-1d6a99b39-6091-a426-e053-dadaa90af4c2Koala Hand Sanitizer - Unscented
75669-0003-22022-01-28C16284748780-1d6a99b39-6091-a426-e053-dadaa90af4c2Koala Hand Sanitizer - Unscented
75669-0003-32022-01-28C16284748780-1d6a99b39-6091-a426-e053-dadaa90af4c2Koala Hand Sanitizer - Unscented
75669-0003-62022-01-28C16284748780-1d6a99b39-6091-a426-e053-dadaa90af4c2Koala Hand Sanitizer - Unscented

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75669-000375669-0003-6, 75669-0003-2, 75669-0003-3

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TRIETHANOLAMINE DODECYLBENZENESULFONATE8HM7ZD48HNIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)71DD5V995LIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
d6ad648e-22aa-49d9-e053-2a95a90a66cbad2b4c83-2c2c-4eee-e053-2a95a90a5d822022-01-28WarningsExact identifier
spl id: d6ad648e-22aa-49d9-e053-2a95a90a66cb
spl set id: ad2b4c83-2c2c-4eee-e053-2a95a90a5d82

Reported adverse events (FAERS/openFDA)#

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