Indications and uses
To help reduce bacteria and viruses on the skin that can potentially cause disease.
Clean Supply Hand Sanitizer
- Manufacturer
- Environmental Applied Technology Corporation
- Effective date
- 2022-07-27
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:56:12
Label at a glance#
ProductClean Supply Hand Sanitizer
Active ingredientALCOHOL
Label structure14 sections
Dosage and administration
• For hands put enough product in the palm to coveryour hand and rub hands together briskly until dry. Supervise children under 6 years of age when using this product to avoid swallowing.
Label contents#
Full prescribing information#
Active Ingredient
Ethyl Alcohol 80%
Purpose
Antiseptic
Uses
To help reduce bacteria and viruses on the skin that can potentially cause disease.
Warnings
Do Not Use On children less than 2 months of age. On open wounds.
Warning
• For external use only.
- Flammable. Keep away from heat or flame.
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 redness occurs.These may be signs of a serious condition.
Keep out of reach of children.
- If swallowed, get medical help or contact a poison control center immediately.
Directions
• For hands put enough product in the palm to coveryour hand and rub hands together briskly until dry.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
• Store between 15 - 30 ̊C (59 - 86 ̊F).
- Avoid freezing and excessive heat above 40 ̊C (104 ̊F).
- May discolor certain fabrics or surfaces.
Inactive Ingredients
Deionized water, Isopropyl Alcohol, Glycol Alcohol, Acrylic Crosspolymer, Trolamine, Hydrogen Peroxide.
59ml
500mL
1892mL
1Gallon
Images
3 mL
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- Clean Supply Hand Sanitizer
- Alcohol
- HYDROGEN PEROXIDE
- WATER
- ISOPROPYL ALCOHOL
- PROPYLENE GLYCOL
- TROLAMINE
- SODIUM POLYACRYLATE (8000 MW)
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 80366-001 | 80366-001-01, 80366-001-02, 80366-001-03, 80366-001-04, 80366-001-05 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HYDROGEN PEROXIDE | BBX060AN9V | IACT |
| WATER | 059QF0KO0R | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| SODIUM POLYACRYLATE (8000 MW) | 285CYO341L | IACT |
| ALCOHOL | 3K9958V90M | 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 |
|---|---|---|---|---|---|---|
| e4cf1def-743c-8baa-e053-2a95a90a23d4 | 751a4708-2720-47fa-b7d8-3ed799964560 | 2022-07-27 | Warnings | e4cf1def-743c-8baa-e053-2a95a90a23d4 751a4708-2720-47fa-b7d8-3ed799964560 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.