FDA.reportPublic FDA data

Cleanse-AF Hand Sanitizer

Manufacturer
California Prison Industry Authority
Effective date
2020-06-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:26:39

Label at a glance#

ProductCleanse-AF Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Pump a small amount of foam into palm of hands. Rub thoroughly over all surfaces of both hands. Rub hands briskly unil dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizing to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

For external use only.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • Deep or puncture wounds
  • Animal bites
  • Serious burns

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes
  • In case of contact, flush eyes with water
  • Do not ingest

OTC - STOP USE SECTION

Stop use and ask a doctor if redness or irritation develops and persists. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children should be supervised when using this product. If swallowed call a Poison Control Center or get medical help right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump a small amount of foam into palm of hands. Rub thoroughly over all surfaces of both hands. Rub hands briskly unil dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

cetrimonium chloride, citric acid, dihydroxyethyl cocamine oxide, glycereth-17 cocoate, lautrimonium chloride, water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

32 FL OZ (946 mL)

NDC 74966-002-32

002002

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
74966-00274966-002-32

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
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
GLYCERETH-17 COCOATE3057VPT0KCIACT

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
1e03be6a-3b0d-5b9c-e063-6394a90a9efda797fcca-823e-2ad3-e053-2a95a90a19a12024-07-24WarningsExact identifier
spl set id: a797fcca-823e-2ad3-e053-2a95a90a19a1

Reported adverse events (FAERS/openFDA)#

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