FDA.reportPublic FDA data

Purgo AF

Manufacturer
Environmental Manufacturing Solutions, LLC.
Effective date
2023-01-19
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 21:40:01

Label at a glance#

ProductPurgo AF
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin

Dosage and administration

Apply to hands liberally. Gently massage into skin until absorbed. Supervise children in the use of this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13% v/v

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only. Do not use in eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if skin irritation develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to hands liberally. Gently massage into skin until absorbed. Supervise children in the use of this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

citric acid, glycerin, lemongrass oil, water

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.

Purpose

OTC - PURPOSE SECTION

Hand sanitizer to help reduce bacteria on the skin

Purgo AF label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Purgo AFPurgo AF

Purgo AF -424 principal display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Purgo AF EucalyptusPurgo AF Eucalyptus

Purgo AF Gel Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Purgo AF Gel 524 labelPurgo AF Gel 524 label

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74869-42474869-424-02, 74869-424-10, 74869-424-11, 74869-424-25, 74869-424-55, 74869-424-27, 74869-424-40
74869-42074869-420-02, 74869-420-10, 74869-420-11, 74869-420-25, 74869-420-55, 74869-420-27, 74869-420-40
74869-52474869-524-02, 74869-524-11, 74869-524-55, 74869-524-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
EAST INDIAN LEMONGRASS OILUP0M8M3VZWIACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
WATER059QF0KO0RIACT
EUCALYPTUS OIL2R04ONI662IACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
POLYSORBATE 806OZP39ZG8HIACT
WATER059QF0KO0RIACT
EUCALYPTUS OIL2R04ONI662IACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)S38J6RZN16IACT

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
f2a0632a-d6e8-101f-e053-2995a90ac6a9a2dffcf7-a16c-bf6d-e053-2995a90a03092023-01-19WarningsExact identifier
spl id: f2a0632a-d6e8-101f-e053-2995a90ac6a9
spl set id: a2dffcf7-a16c-bf6d-e053-2995a90a0309

Reported adverse events (FAERS/openFDA)#

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