Dosage and administration
Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision.
Dr. Talbots
- Manufacturer
- Talbot’s Pharmaceuticals Family Products, LLC.
- Effective date
- 2025-01-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 00:51:32
Label at a glance#
ProductDr. Talbots
Active ingredientALCOHOL
Label structure11 sections
Storage and handling
Store at normal room temperature May discolor certain fabrics May be harmful to wood finishes and plastics
Label contents#
Full prescribing information#
Purpose
Antiseptic, Hand Sanitizer
Use
To help reduce bacteria on the skin that could cause disease. Recommended for repeated use.
Warnings
For external use only. Flammable. Keep away from heat or flame
OTC - WHEN USING SECTION
When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or redness develops, condition persists for more than 72 hours consult a doctor.
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.
Directions
- Wet hands thoroughly with product and allow to dry without wiping.
- For children under 6, use only under adult supervision.
Other information
- Store at normal room temperature
- May discolor certain fabrics
- May be harmful to wood finishes and plastics
Inactive ingredients
aqua, glycerin, carbomer, aminomethyl propanol
OTC - ACTIVE INGREDIENT SECTION
Ethyl Alcohol 75%
Package Label - Principal Display Panel
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70797-160-01 | Dr. Talbots | 50 mL in 1 BOTTLE | GEL | 50 | 4 | |
| 70797-160-02 | Dr. Talbots | 250 mL in 1 BOTTLE, PUMP | GEL | 250 | 4 | |
| 70797-160-03 | Dr. Talbots | 500 mL in 1 BOTTLE, PUMP | GEL | 500 | 4 | |
| 70797-160-04 | Dr. Talbots | 1000 mL in 1 BOTTLE, PUMP | GEL | 1000 | 4 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Dr. Talbots
- Ethyl Alcohol
- GLYCERIN
- WATER
- ALCOHOL
- AMINOMETHYL PROPANEDIOL
- CARBOMER 934
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70797-160 | 70797-160-01, 70797-160-02, 70797-160-03, 70797-160-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| AMINOMETHYL PROPANEDIOL | CZ7BU4QZJZ | IACT |
| CARBOMER 934 | Z135WT9208 | 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 |
|---|---|---|---|---|---|---|
| Dr. Talbots | ETHYL ALCOHOL | Talbots Pharmaceuticals Family Products, LLC. | a6a94205-a9ff-7709-e053-2995a90a066b | 2025-01-08 | Warnings | 70797-160-02 70797-160-01 70797-160-03 70797-160-04 70797-160 70797016003 70797016002 70797016001 70797016004 2b380620-3e8e-77b0-e063-6394a90a9442 a6a94205-a9ff-7709-e053-2995a90a066b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.