PURELL Advanced Hand Sanitizer be Blissful

Manufacturer
GOJO Industries, Inc.
Effective date
2026-03-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:51:54

Label at a glance#

ProductPURELL Advanced Hand Sanitizer be Blissful
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), Red 40 (CI 16035), Yellow 6 (CI 15985)

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 Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21749-029-01PURELL Advanced Hand Sanitizer be Blissful30 mL in 1 PACKAGEGEL304
21749-029-02PURELL Advanced Hand Sanitizer be Blissful59 mL in 1 PACKAGEGEL594
21749-029-04PURELL Advanced Hand Sanitizer be Blissful118 mL in 1 PACKAGEGEL1184
21749-029-08PURELL Advanced Hand Sanitizer be Blissful236 mL in 1 PACKAGEGEL2364
21749-029-10PURELL Advanced Hand Sanitizer be Blissful295 mL in 1 PACKAGEGEL2954
21749-029-12PURELL Advanced Hand Sanitizer be Blissful354 mL in 1 PACKAGEGEL3544
21749-029-16PURELL Advanced Hand Sanitizer be Blissful473 mL in 1 PACKAGEGEL4734
21749-029-20PURELL Advanced Hand Sanitizer be Blissful591 mL in 1 PACKAGEGEL5914
21749-029-45PURELL Advanced Hand Sanitizer be Blissful450 mL in 1 PACKAGEGEL4504

Products#

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NDC Codes#

Ingredients#

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

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

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 BlissfulALCOHOLGOJO Industries, Inc.cebd0adb-dc26-407f-a290-418e0e206aea2026-03-27WarningsExact identifier
ndc (package): 21749-029-20
ndc (package): 21749-029-12
ndc (package): 21749-029-04
ndc (package): 21749-029-08
ndc (package): 21749-029-45
ndc (package): 21749-029-02
ndc (package): 21749-029-01
ndc (package): 21749-029-10
ndc (package): 21749-029-16
ndc (product): 21749-029
ndc11 (package): 21749002908
ndc11 (package): 21749002916
ndc11 (package): 21749002920
ndc11 (package): 21749002901
ndc11 (package): 21749002945
ndc11 (package): 21749002912
ndc11 (package): 21749002902
ndc11 (package): 21749002904
ndc11 (package): 21749002910
spl id: 4e087c55-325e-7d5e-e063-6394a90a916a
spl set id: cebd0adb-dc26-407f-a290-418e0e206aea

Reported adverse events (FAERS/openFDA)#

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