OTC - ACTIVE INGREDIENT SECTION
Ethyl Alcohol 62% v/v.......Antibacterial Agent
eZFoam Foaming Alcohol Hand Sanitizer
- Manufacturer
- Kutol Products Company | Kutol Products Company.
- Effective date
- 2024-12-18
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- full-release
- Hydrated at
- 2026-06-01 00:44:28
Label at a glance#
ProducteZFoam Foaming Alcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
Water, AMP-C8-18 Perfluoroalkylethyl Phosphate, Glycerin.
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.
FLAMMABLE. Keep away from heat or flames.
Avoid contact with eyes. If eye 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 eye 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.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50865-688-03 | eZFoam Foaming Alcohol Hand Sanitizer | 213125 mL in 1 DRUM | SOLUTION | 213125 | 6 | |
| 50865-688-09 | eZFoam Foaming Alcohol Hand Sanitizer | 3785 mL in 1 JUG | SOLUTION | 3785 | 6 | |
| 50865-688-17 | eZFoam Foaming Alcohol Hand Sanitizer | 50 mL in 1 BOTTLE, PLASTIC | SOLUTION | 50 | 6 | |
| 50865-688-24 | eZFoam Foaming Alcohol Hand Sanitizer | 1000 mL in 1 BAG | SOLUTION | 1000 | 6 | |
| 50865-688-41 | eZFoam Foaming Alcohol Hand Sanitizer | 1000 mL in 1 BAG | SOLUTION | 1000 | 6 | |
| 50865-688-50 | eZFoam Foaming Alcohol Hand Sanitizer | 1200 mL in 1 BAG | SOLUTION | 1200 | 6 | |
| 50865-688-78 | eZFoam Foaming Alcohol Hand Sanitizer | 950 mL in 1 BOTTLE, PLASTIC | SOLUTION | 950 | 6 | |
| 50865-688-91 | eZFoam Foaming Alcohol Hand Sanitizer | 532 mL in 1 BOTTLE, PLASTIC | SOLUTION | 532 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ALCOHOL | ACTIVE INGREDIENT | 3K9958V90M | 1 | |
| ALCOHOL | ACTIVE MOIETY | 3K9958V90M | 1 | |
| AMINOMETHYLPROPANOL (PERFLUORO-C6-C12 ETHYL)PHOSPHATE | INACTIVE INGREDIENT | QCD5R22RNT | 1 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- eZFoam Foaming Alcohol Hand Sanitizer
- Foaming Hand Sanitizer
- WATER
- GLYCERIN
- AMINOMETHYLPROPANOL (PERFLUORO-C6-C12 ETHYL)PHOSPHATE
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50865-688 | 50865-688-03, 50865-688-09, 50865-688-17, 50865-688-24, 50865-688-41, 50865-688-78, 50865-688-91, 50865-688-50 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| AMINOMETHYLPROPANOL (PERFLUORO-C6-C12 ETHYL)PHOSPHATE | QCD5R22RNT | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| GLYCERIN | GLYCERIN | PDC6A3C0OX | SOLUTION / TOPICAL | 1971 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | SOLUTION / TOPICAL | 1971 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | SOLUTION / TOPICAL | 1971 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | SOLUTION / TOPICAL | 1971 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | SOLUTION / TOPICAL | 1971 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | SOLUTION / TOPICAL | 1971 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | SOLUTION / TOPICAL | 1971 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | SOLUTION / TOPICAL | 1971 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | SOLUTION / TOPICAL | 1971 mg |
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 |
|---|---|---|---|---|---|---|
| eZFoam Foaming Alcohol Hand Sanitizer | FOAMING HAND SANITIZER | Kutol Products Company | 1f56b4c5-d703-4193-83a8-3be815c8acda | 2024-12-18 | Warnings | 50865-688-03 50865-688-17 50865-688-91 50865-688-09 50865-688-78 50865-688-24 50865-688-50 50865-688-41 50865-688 50865068850 50865068809 50865068891 50865068841 50865068817 50865068824 50865068803 50865068878 298e167d-7005-98da-e063-6294a90a07ba 1f56b4c5-d703-4193-83a8-3be815c8acda |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.