KLEANMANN - Hand Sanitizer and Surface Disinfectant

Manufacturer
Lamer Group LLC
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:17:33

Label at a glance#

ProductKLEANMANN - Hand Sanitizer and Surface Disinfectant
Active ingredientBENZALKONIUM CHLORIDE, DIDECYLDIMONIUM CHLORIDE
Label structure10 sections

Dosage and administration

For hand disinfection, rub the solution carefully into your palms for 30 seconds. Clean and disinfect frequently touched objects and surfaces by spraying directly on them.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is a hand sanitizer and surface disinfectant manufactured, tested, and registered in the EU.

The hand sanitizer is manufactured using only the following ingredients in the preparation of the product (percentage in final product formulation):

  1. BAC (Benzalkonium Chloride) less than 1.6%
  2. DDAC (Didecyldimonium Chloride) less than 0.4%
  3. Purified water

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

EU OTC InformationEU OTC Information

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

BAC (Benzalkonium Chloride) less than 1.6% v/v Purpose: Skin Antiseptic:
DDAC (Didecyldimonium Chloride) less than 0.4% v/v Purpose: Food Contact Sanitizer

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer Spray and Surface Disinfectant

Use

INDICATIONS & USAGE SECTION

For hand and surface sanitizing to decrease harmful bacteria and viruses on the skin or frequently touched objects. Recommended for repeated use.

Do not use

OTC - DO NOT USE SECTION

  • Do not use in eyes. If contact occurs, flush thoroughly with water.

OTC - STOP USE SECTION

Stop use and contact a doctor if redness or irritation develops and persists for more than 72 hours.

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

For hand disinfection, rub the solution carefully into your palms for 30 seconds. Clean and disinfect frequently touched objects and surfaces by spraying directly on them.

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

120 ml NDC: 00000-000-00

120ml Label120ml Label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80472-00180472-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
05e4d504-a233-a262-e063-6294a90a3b94ae01acc1-979b-7253-e053-2a95a90aee992023-09-21WarningsExact identifier
spl set id: ae01acc1-979b-7253-e053-2a95a90aee99

Reported adverse events (FAERS/openFDA)#

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