Indications and uses
for hand sanitizing to decrease bacteria on the skin recommended for repeated use
Benzalkonium Chloride
- Manufacturer
- ALO NEW YORK LLC
- Effective date
- 2025-12-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- full-release
- Hydrated at
- 2026-06-01 01:20:25
Label at a glance#
ProductBenzalkonium Chloride
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections
Dosage and administration
adults and children 2 years and over: apply to hands: allow to dry without wiping children under 2 years: ask a doctor before use. To dispense : Peel back fron label slowly. Remove wipes. To reseal : Firmly rub thumb over label. Dispose of wipe in trash. Do not flush.
Label contents#
Full prescribing information#
Active ingredients
Benzalkonium Chloride 0.13%
Purpose
Antimicrobial
Uses
- for hand sanitizing to decrease bacteria on the skin
- recommended for repeated use
Warnings
For external use only.
Do not use
if you are allergic to any of these ingredients.
When using this product
avoid contact with eyes. In case of contact, flush eyes with water.
Stop use and ask a doctor
if irritation or redness develops, or if condition persists for more than 72 hours.
Keep out of the reach of children.
If swallowed, get medical help or contact Poison Control Center right away.
Directions
- adults and children 2 years and over: apply to hands: allow to dry without wiping
- children under 2 years: ask a doctor before use.
- To dispense: Peel back fron label slowly. Remove wipes.
- To reseal: Firmly rub thumb over label. Dispose of wipe in trash. Do not flush.
Other information
store below 95
- store below 95°F (35°C).
- keep closed tightly
- may discolor certain fabrics or surfaces.
Inactive ingredients
Purified Water, Decyl Glucoside, Aloe Barbadensis (Aloe) Leaf Extract, Phenoxyethanol, Citric Acid, Sodium Benzoate, Potassium Sorbate, Eucalyptus Globulus Oil, Mentha Piperita (Peppermint) Oil.
Principal Display Panel
ALO
20 Skin-Softening Sanitizing Hand Wipes
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82355-551-01 | Benzalkonium Chloride | 20 in 1 PACKAGE | CLOTH | 20 | 5 | |
| 82355-551-01 | Benzalkonium Chloride | 1 mg in 1 PACKAGE | CLOTH | 1 | 5 |
Products#
Every source-derived product name is available through these pages.
- Benzalkonium Chloride
- Sanitizing Hand Wipes
- WATER
- ALOE VERA LEAF
- PHENOXYETHANOL
- SODIUM BENZOATE
- DECYL GLUCOSIDE
- CITRIC ACID MONOHYDRATE
- POTASSIUM SORBATE
- BENZALKONIUM
- BERGAMOT OIL
- ORANGE OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 82355-551 | 82355-551-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| DECYL GLUCOSIDE | Z17H97EA6Y | IACT |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| POTASSIUM SORBATE | 1VPU26JZZ4 | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| BERGAMOT OIL | 39W1PKE3JI | IACT |
| ORANGE OIL | AKN3KSD11B | IACT |
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 |
|---|---|---|---|---|---|---|
| Benzalkonium Chloride | SANITIZING HAND WIPES | ALO NEW YORK LLC | d3d95355-3af7-43e3-e053-2a95a90a0fa4 | 2025-12-05 | Warnings | 82355-551-01 82355-551 82355055101 45390be0-fcf5-3640-e063-6394a90a2697 d3d95355-3af7-43e3-e053-2a95a90a0fa4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.