Advanced

Manufacturer
Freshorize Ltd | Derma Care Research Labs, LLC | GOJO Industries, Inc.
Effective date
2020-08-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:25:48

Label at a glance#

ProductAdvanced Purell
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

OTC - PURPOSE SECTION


Antimicrobial

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

WARNINGS SECTION

Flammable-keep away from fire or flame. For external use only. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Isopropyl Alcohol, PEG-12 Dimethicone, Caprylyl Glycol, Glycerin, Propylene Glycol, Isopropyl Myristate, Tocopheryl Acetate, Fragrance.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN1
616805ethanol 0.7 ML/ML Topical FoamSCD1
616805ethanol 70 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52305-940-102023-01-30C16284748780-1f386c64a-263d-0266-e053-dadaa90a7c1aHand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52305-940-10AdvancedPurell300 mL in 1 BOTTLE, PUMPLIQUID3001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52305-940ADVANCED PURELL (ETHYL ALCOHOL) LIQUID [FRESHORIZE LTD]1Legacy NDC, 1 package rows20200826_ada5e199-7816-9c4c-e053-2a95a90a4fc0.zip

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
52305-94052305-940-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
ada5e199-7815-9c4c-e053-2a95a90a4fc0ada5e199-7816-9c4c-e053-2a95a90a4fc02020-08-24WarningsExact identifier
spl id: ada5e199-7815-9c4c-e053-2a95a90a4fc0
spl set id: ada5e199-7816-9c4c-e053-2a95a90a4fc0

Reported adverse events (FAERS/openFDA)#

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