OTC - ACTIVE INGREDIENT SECTION
Benzalkonium Chloride 0.0026%
Instant Foaming Hand Sanitizer
- Manufacturer
- Kimball Midwest | KUTOL PRODUCTS COMPANY
- Effective date
- 2023-12-12
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 8
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:18:35
Label at a glance#
ProductInstant Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
Water, Fragrance, Aloe Barbadensis Leaf, Tocopheryl Acetate, Cocamidopropyl Betaine, Propylene Glycol, Phenoxyethanol, PEG-7 Glyceryl Cocoate, Tetrasodium EDTA.
OTC - PURPOSE SECTION
Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.
WARNINGS SECTION
For external use only.
Avoid contact with eyes. If contact occurs, flush with water.
Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.
Keep out of reach of children. If swallowed, contact a physician or poison control center.
DOSAGE & ADMINISTRATION SECTION
To decrease bacteria on skin, apply small amount to palm. Briskly rub, covering hands with product until dry.
INDICATIONS & USAGE SECTION
Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.
Avoid contact with eyes. If contact occurs, flush with water.
Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.
Keep out of reach of children. If swallowed, contact a physician or poison control center.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, contact a physician or poison control center.
Packaging
Products#
Every source-derived product name is available through these pages.
- Instant Foaming Hand Sanitizer
- Benzalkonium chloride
- EDETATE SODIUM
- COCAMIDOPROPYL BETAINE
- PEG-7 GLYCERYL COCOATE
- PROPYLENE GLYCOL
- PHENOXYETHANOL
- ALOE VERA LEAF
- .ALPHA.-TOCOPHEROL ACETATE, DL-
- BENZALKONIUM
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 66608-207 | 66608-207-78, 66608-207-17 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| EDETATE SODIUM | MP1J8420LU | IACT |
| COCAMIDOPROPYL BETAINE | 5OCF3O11KX | IACT |
| PEG-7 GLYCERYL COCOATE | VNX7251543 | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| .ALPHA.-TOCOPHEROL ACETATE, DL- | WR1WPI7EW8 | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| d24760bb-8461-49f6-b2a9-155f9c7c55cc | 4c5f528e-91ae-1c90-e054-00144ff8d46c | 2023-12-12 | Warnings | d24760bb-8461-49f6-b2a9-155f9c7c55cc 4c5f528e-91ae-1c90-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.