Indications and uses
• To decrease bacteria on the skin. • Recommended for repeated use. • For use when soap and water are not available
Molchem hand purifier
- Manufacturer
- MOL BELTING SYSTEMS, INC | Mol Belting Systems Inc
- Effective date
- 2023-06-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:30:01
Label at a glance#
ProductMolchem hand purifier
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections
Dosage and administration
• Place enough product on hands to cover all surfaces. Rub hands together. • Supervise children under 6 years of age when using this product to avoid swallowing.
Label contents#
Full prescribing information#
Warnings
For external use only.
When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse thoroughly
with water.
Stop use and ask a doctor if irritation or rash occurs. This may be a sign of a serious condition.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Other information
Store in dry place between 35° and 103°F
Directions
• Place enough product on hands to cover all surfaces. Rub hands together.
• Supervise children under 6 years of age when using this product to avoid swallowing.
Uses
• To decrease bacteria on the skin.
• Recommended for repeated use.
• For use when soap and water are not available
Inactive ingredients
Deionized Water, Propylene glycol, Triethylene glycol, Phospholipids Complex, Organo Silane Quaternaries
Active ingredient
Benzalkonium Chloride 0.13%
Purpose
Antiseptic
Product label
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- Molchem hand purifier
- BENZALKONIUM CHLORIDE
- DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE
- PROPYLENE GLYCOL
- TRIETHYLENE GLYCOL
- PEG-75 LANOLIN
- WATER
- BENZALKONIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 80606-001 | 80606-001-01, 80606-001-02, 80606-001-03, 80606-001-04, 80606-001-05, 80606-001-06, 80606-001-07 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE | IQ36O85WQ4 | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| TRIETHYLENE GLYCOL | 3P5SU53360 | IACT |
| PEG-75 LANOLIN | 09179OX7TB | IACT |
| WATER | 059QF0KO0R | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 2a49ea0f-d6fd-b0d8-e063-6394a90aed64 | 303b5ce9-9715-4291-a899-649d1d70fc95 | 2024-12-27 | Warnings | 303b5ce9-9715-4291-a899-649d1d70fc95 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.