Ty-D Gel Hand Sanitizer
- Manufacturer
- Willert Manufacturing Company, LLC
- Effective date
- 2021-10-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:31:03
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Ethyl Alcohol 69%v/v ...Antiseptic
OTC - ASK DOCTOR SECTION
Stop use and ask a doctor if ■ irritation and redness develop
■ condition persists for more than 72 hours.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a
Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Uses ■ to decrease bacteria on the skin that could cause
disease ■ recommended for repeated use
OTC - QUESTIONS SECTION
Questions? 1-833-907-2438
OTC - WHEN USING SECTION
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.
WARNINGS SECTION
Warnings
For external use only: hands
Flammable. Keep away from fire or flame.
INACTIVE INGREDIENT SECTION
Inactive Ingredients water, glycerin, hydroxypropyl methylcellulose, cetyl lactate, lauryl lactate and myristyl lactate
INSTRUCTIONS FOR USE SECTION
Directions ■ wet hands thoroughly with product and allow to dry without wiping ■ for chi ldren under 6, use only under adult supervision
not recommended for infants
OTHER SAFETY INFORMATION
Other Information ■ do not store above 105° F■ may discolor some fabrics ■ harmful to wood finishes and plastics
INDICATIONS & USAGE SECTION
Uses: to decrease bacteria on the skin that could cause diseease. Reccomended for repeated use.
OTC - PURPOSE SECTION
Purpose: Antiseptic
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
946ml NDC 73830-211-32
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Ty-D Gel Hand Sanitizer
- Ethyl Alcohol
- MYRISTYL LACTATE
- ALCOHOL
- HYPROMELLOSE, UNSPECIFIED
- LAURYL LACTATE
- GLYCERIN
- WATER
- CETYL LACTATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73830-211 | 73830-211-32, 73830-211-33 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MYRISTYL LACTATE | 1D822OC34X | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
| LAURYL LACTATE | G5SU0BFK7O | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| WATER | 059QF0KO0R | IACT |
| CETYL LACTATE | A7EVH2RK4O | 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 |
|---|---|---|---|---|---|---|
| cef308d4-a9ed-7564-e053-2a95a90a9ccf | a3ce913a-e402-75e9-e053-2a95a90a7b91 | 2021-10-22 | Warnings | cef308d4-a9ed-7564-e053-2a95a90a9ccf a3ce913a-e402-75e9-e053-2a95a90a7b91 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

