FDA.reportPublic FDA data

PURELL Advanced Hand Sanitizer be Vibrant

Manufacturer
GOJO Industries, Inc.
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:32:30

Label at a glance#

ProductPURELL Advanced Hand Sanitizer be Vibrant
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), Yellow 5 (CI 19140)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN4
581662ethanol 0.7 ML/ML Topical GelSCD4
581662ethanol 70 % Topical GelSY4
581662ethyl alcohol 70 % Topical GelSY4

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21749-028-01PURELL Advanced Hand Sanitizer be Vibrant30 mL in 1 PACKAGEGEL304
21749-028-02PURELL Advanced Hand Sanitizer be Vibrant59 mL in 1 PACKAGEGEL594
21749-028-04PURELL Advanced Hand Sanitizer be Vibrant118 mL in 1 PACKAGEGEL1184
21749-028-08PURELL Advanced Hand Sanitizer be Vibrant236 mL in 1 PACKAGEGEL2364
21749-028-10PURELL Advanced Hand Sanitizer be Vibrant295 mL in 1 PACKAGEGEL2954
21749-028-12PURELL Advanced Hand Sanitizer be Vibrant354 mL in 1 PACKAGEGEL3544
21749-028-16PURELL Advanced Hand Sanitizer be Vibrant473 mL in 1 PACKAGEGEL4734
21749-028-20PURELL Advanced Hand Sanitizer be Vibrant591 mL in 1 PACKAGEGEL5914
21749-028-45PURELL Advanced Hand Sanitizer be Vibrant450 mL in 1 PACKAGEGEL4504

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
21749-02821749-028-01, 21749-028-02, 21749-028-04, 21749-028-08, 21749-028-10, 21749-028-12, 21749-028-45, 21749-028-16, 21749-028-20

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
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 YELLOW NO. 5I753WB2F1MIACT
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
PURELL Advanced Hand Sanitizer be VibrantALCOHOLGOJO Industries, Inc.3a991a7f-1289-4aeb-82f9-8cebd6a389b52026-01-12WarningsExact identifier
ndc (package): 21749-028-10
ndc (package): 21749-028-12
ndc (package): 21749-028-04
ndc (package): 21749-028-01
ndc (package): 21749-028-02
ndc (package): 21749-028-16
ndc (package): 21749-028-08
ndc (package): 21749-028-45
ndc (package): 21749-028-20
ndc (product): 21749-028
ndc11 (package): 21749002802
ndc11 (package): 21749002816
ndc11 (package): 21749002812
ndc11 (package): 21749002810
ndc11 (package): 21749002845
ndc11 (package): 21749002820
ndc11 (package): 21749002801
ndc11 (package): 21749002808
ndc11 (package): 21749002804
spl id: 48366d7a-55a5-901e-e063-6294a90a677d
spl set id: 3a991a7f-1289-4aeb-82f9-8cebd6a389b5

Reported adverse events (FAERS/openFDA)#

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