Bortek E-3 Foaming Hand Sanitizer
- Manufacturer
- Bortek Industries
- Effective date
- 2023-01-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:39:49
Label at a glance#
ProductBortek E-3 Foaming Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active ingredient
Alcohol 70% v/v
OTC - PURPOSE SECTION
Purpose
Antiseptic
INDICATIONS & USAGE SECTION
Uses
To decrease bacteria on the skin after changing diapers, assisting ill persons or before contact with a person under medical care or treatment.
WARNINGS SECTION
Warnings
For external use only.
Flammable, keep away from fire or flame
OTC - WHEN USING SECTION
When using this product, keep away from eyes. In case of eye contact, rinse thoroughly with water.
OTC - STOP USE SECTION
Stop use and ask a doctor if if irritation or redness develop or last 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 immediately.
DOSAGE & ADMINISTRATION SECTION
Directions
- Apply liberally to hands to cover all surfaces, including the area under the fingernails
- Rub hands together until dry
INACTIVE INGREDIENT SECTION
Inactive ingredients
Benzalkonium chloride, chlorhexidine gluconate, isopropyl alcohol, PEG 10 dimethicone, phenoxyethanol, polyethylene oxid 600000, polyquaternium 10, water.
SPL UNCLASSIFIED SECTION
800.626.7835
BortekShop.com
Distributed by Bortek Industries, Inc., Mechanicsburg, PA 17055
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Bortek® INDUSTRIES, INC.
Alcohol 70% Antiseptic
E-3 FOAMING HAND SANITIZER
33.8 fl oz (1000 mL)
Products#
Every source-derived product name is available through these pages.
- Bortek E-3 Foaming Hand Sanitizer
- Ethanol
- BENZALKONIUM CHLORIDE
- CHLORHEXIDINE GLUCONATE
- ISOPROPYL ALCOHOL
- PEG-10 DIMETHICONE (600 CST)
- POLYETHYLENE OXIDE 600000
- PHENOXYETHANOL
- POLYQUATERNIUM-10 (1000 MPA.S AT 2%)
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 81731-203 | 81731-203-01, 81731-203-11 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| CHLORHEXIDINE GLUCONATE | MOR84MUD8E | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | IACT |
| PEG-10 DIMETHICONE (600 CST) | 8PR7V1SVM0 | IACT |
| POLYETHYLENE OXIDE 600000 | 2126FD486L | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| POLYQUATERNIUM-10 (1000 MPA.S AT 2%) | GMR4PEN8PK | 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 |
|---|---|---|---|---|---|---|
| f278dd67-0c7a-39c5-e053-2995a90a9398 | bfcceb3d-4b06-5e3e-e053-2a95a90a46e1 | 2023-01-17 | Warnings | f278dd67-0c7a-39c5-e053-2995a90a9398 bfcceb3d-4b06-5e3e-e053-2a95a90a46e1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.