HAND SANITIZER
- Manufacturer
- Total Resources International Inc.
- Effective date
- 2022-12-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- full-release
- Hydrated at
- 2026-05-31 23:52:19
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient Purpose
Ethyl Alcohol 66.5% v/v....................Antiseptic
OTC - PURPOSE SECTION
Use: For handwashing to decrease bacteria on skin without soap and water.
WARNINGS SECTION
Warnings For external use only
Flammable, keep away from fire or flame
OTC - DO NOT USE SECTION
Do not use •in the eyes if happens, rinse thoroughly with water.
OTC - STOP USE SECTION
Stop use, ask a doctor if irritation develops and persists for 72 hours.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, seek medical help or contact a Poison Control Center immediately.
INDICATIONS & USAGE SECTION
Directions wet hands and wrists thoroughly with product and allow to dry without wiping supervise children while using this product
OTHER SAFETY INFORMATION
Other Information store at room temperature 59°- 86°F ( 15°- 30°C )
INACTIVE INGREDIENT SECTION
Inactive ingredient aloe vera*, carbomer*, D&C green #5*, D&C yellow #10*, fragrance *, triethanolamine*, water* may contain
OTC - QUESTIONS SECTION
Questions? Call 1-888-771-7824
DOSAGE & ADMINISTRATION SECTION
For External Use Only
HAND SANITIZER
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 55550-108-08 | 2024-01-30 | C162847 | 48780-1 | 1030e365-50de-111a-e063-dadaa90a10e2 | Hand Sanitizer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55550-108-08 | HAND SANITIZER08 | 1.5 mL in 1 POUCH | PATCH | 1.5 | 6 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- HAND SANITIZER 08
- ETHYL ALCOHOL
- ALOE
- TROLAMINE
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55550-108 | 55550-108-08 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALOE | V5VD430YW9 | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| ef2cda8f-157f-4f93-e053-2a95a90aebb5 | bbf69bef-8519-493d-e053-2a95a90a6547 | 2022-12-06 | Warnings | ef2cda8f-157f-4f93-e053-2a95a90aebb5 bbf69bef-8519-493d-e053-2a95a90a6547 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
