FDA.reportPublic FDA data

Active ingredient

Manufacturer
Clorox Purell ProCare, LLC
Effective date
2026-11-10
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-11-14 03:02:52

Label at a glance#

ProductPURELL Advanced Hand Sanitizer be Peaceful
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children under 6 years of age shodl be supervised when 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

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

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

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts

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

  • Place enough product in your palm to thoroughly cover your hands
  • Rub hands together briskly until dry
  • Children under 6 years of age shodl be supervised when 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 (Aqua), Isopropyl Alcohol, Caprylyl glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Blue 1 (CI 42090), Red 40 (CI 16035)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21749-02721749-027-01, 21749-027-02, 21749-027-04, 21749-027-08, 21749-027-10, 21749-027-12, 21749-027-45, 21749-027-16, 21749-027-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
CAPRYLYL GLYCOL00YIU5438UIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C RED NO. 40WZB9127XOAIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42026-01-12full-release2026-06-01 01:32:32

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
PURELL Advanced Hand Sanitizer be PeacefulALCOHOLGOJO Industries, Inc.45810c51-8738-4b8a-8d8f-46b4b41dbe932026-01-12WarningsExact identifier
ndc (package): 21749-027-16
ndc (package): 21749-027-45
ndc (package): 21749-027-10
ndc (package): 21749-027-20
ndc (package): 21749-027-12
ndc (package): 21749-027-04
ndc (package): 21749-027-08
ndc (package): 21749-027-02
ndc (package): 21749-027-01
ndc (product): 21749-027
ndc11 (package): 21749002701
ndc11 (package): 21749002720
ndc11 (package): 21749002704
ndc11 (package): 21749002702
ndc11 (package): 21749002712
ndc11 (package): 21749002745
ndc11 (package): 21749002710
ndc11 (package): 21749002716
ndc11 (package): 21749002708
spl set id: 45810c51-8738-4b8a-8d8f-46b4b41dbe93

Reported adverse events (FAERS/openFDA)#

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