FDA.reportPublic FDA data

Afia Alcohol-Free Foaming Hand Sanitizer

Manufacturer
National Chemical Laboratories, Inc.
Effective date
2023-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:31:58

Label at a glance#

ProductAfia Alcohol-Free Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

Pump a small amount of foam into palm of hand Rub thoroughly over all surfaces of both hands Rub hands together briskly until dry

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient. Purpose

Benzalkonium Chloride 0.13%....... Antimicrobial.

Uses

OTC - PURPOSE SECTION

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

Warnings:

WARNINGS SECTION

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persist for more than 72 hours.

Directions

DOSAGE & ADMINISTRATION SECTION

Pump a small amount of foam into palm of hand

Rub thoroughly over all surfaces of both hands

Rub hands together briskly until dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Fragrance, Glyceth-17 Cocoate, Citric Acid

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Afia Alcohol-Free Foaming Hand Sanitizer

Afia Alcohol-Free Hand SanitizerAfia Alcohol-Free Hand Sanitizer

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71023-045-292024-01-30C16284748780-11030e365-0ffd-111a-e063-dadaa90a10e2Listing of Alcohol-Free Foaming Hand Sanitizer in multiple packages
71023-045-322024-01-30C16284748780-11030e365-0ffd-111a-e063-dadaa90a10e2Listing of Alcohol-Free Foaming Hand Sanitizer in multiple packages
71023-045-572024-01-30C16284748780-11030e365-0ffd-111a-e063-dadaa90a10e2Listing of Alcohol-Free Foaming Hand Sanitizer in multiple packages

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71023-04571023-045-57, 71023-045-29, 71023-045-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
GLYCERETH-17 COCOATE3057VPT0KCIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
WATER059QF0KO0RIACT

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
1c5988b4-16d5-be18-e063-6294a90ad3d5fa690ebf-a7ae-558f-e053-6294a90a3c752024-07-03WarningsExact identifier
spl set id: fa690ebf-a7ae-558f-e053-6294a90a3c75

Reported adverse events (FAERS/openFDA)#

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