FDA.reportPublic FDA data

Advanced Hand Sanitizer

Manufacturer
Kareway Product, Inc.
Effective date
2020-04-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:33:18

Label at a glance#

ProductAdvanced Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

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

Storage and handling

Store below 110ºF (43ºC)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin

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 eyes thoroughly with water

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

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 or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other Information

STORAGE AND HANDLING SECTION

  • Store below 110ºF (43ºC)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Aminomethyl Propano, Carbomer, Citrus Aurantium Dulcis (Orange) Fruit Extract, Fragrance, Propylene Glycol, 1,2-Hexanediol, Denatonium Benzoate

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67510-0132-12022-01-28C16284748780-1d6a99b39-5611-a426-e053-dadaa90af4c2Pure-Aid Advanced Hand Sanitizer
67510-0132-82022-01-28C16284748780-1d6a99b39-5611-a426-e053-dadaa90af4c2Pure-Aid Advanced Hand Sanitizer

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67510-013267510-0132-8, 67510-0132-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)HHT01ZNK31IACT
ORANGE OILAKN3KSD11BIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
ALCOHOL3K9958V90MACTIB

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
a4895905-d5bb-63b4-e053-2995a90ae46ea4893afe-aa87-1eda-e053-2a95a90a5e682020-04-30WarningsExact identifier
spl id: a4895905-d5bb-63b4-e053-2995a90ae46e
spl set id: a4893afe-aa87-1eda-e053-2a95a90a5e68

Reported adverse events (FAERS/openFDA)#

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