OTC - ACTIVE INGREDIENT SECTION
Ethyl Alcohol 77.3% v/v
Ethyl Alcohol 77.3% v/v
WATER, FRAGRANCE, T-BUTYL ALCOHOL, DENATONIUM BENZOATE.
Antibacterial
To decrease bacteria on the skin.
If product is swallowed, get medical help or contact a poison control center right away.
For external use only.
Flammable. Keep away from fire or flame.
When using this product
keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Avoid contact with broken skin.
Do not inhale or ingest.
Stop use and ask a doctor if
Irritation or redness develops.
Condition persists for more than 72 hours.
Keep out of reach of children.
If product is swallowed, get medical helpor contact a poison control center right away.
Spray hands with product to cover all surfaces and allow to dry without wiping.
For adult use only.
Do not store above 105 °F
May discolor some fabrics
Harmful to wood finishes and plastics
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 85161-178 | 85161-178-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
| FRAGRANCE 13576 | 5EM498GW35 | IACT |
| T-BUTYL ALCOHOL | MD83SFE959 | IACT |
| DENATONIUM BENZOATE | 4YK5Z54AT2 | IACT |
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.
Adverse event summaries are temporarily unavailable. Other product information remains available.