Indications and uses
For hand washing to decrease bacteria on the skin
Alcohol-Free Antibacterial Hand Sanitizer Gel
- Manufacturer
- Tekweld Solutions, Inc.
- Effective date
- 2021-07-16
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:39:36
Label at a glance#
ProductAlcohol Free Antibacterial Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections
Dosage and administration
For adults and children 2 years and older. Apply about a thumbnail size amount on palms and rub hands thoroughly until dry.
Contacts and useful links#
Label contents#
Full prescribing information#
Active Ingredient
Benzalkonium Chloride 0.10%
Purpose
Antimicrobial
Uses
For hand washing to decrease bacteria on the skin
Warnings
For external use only.
Avoid contact with eyes. In case of contact with eyes, flush thoroughly with water.
Stop use and ask doctor
if skin irritation and redness develops.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
For adults and children 2 years and older. Apply about a thumbnail size amount on palms and rub hands thoroughly until dry.
Inactive Ingredients
Water (Aqua), Glycerin, Hydroxyethylcellulose, Allantoin, Disodium EDTA.
Drug Questions:
877-254-2281
Alcohol-Free Antibacterial Hand Sanitizer Gel 1 oz (71160-190-01)
Alcohol-Free Antibacterial Hand Sanitizer Gel 2 oz (71160-190-02)
Alcohol-Free Antibacterial Hand Sanitizer Gel 4 oz (71160-190-04)
Alcohol-Free Antibacterial Hand Sanitizer Gel 8 oz (71160-190-08)
Alcohol-Free Antibacterial Hand Sanitizer Gel 16 oz(71160-190-16)
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- Alcohol Free Antibacterial Hand Sanitizer
- BENZALKONIUM CHLORIDE
- WATER
- GLYCERIN
- ALLANTOIN
- EDETATE DISODIUM ANHYDROUS
- BENZALKONIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71160-190 | 71160-190-01, 71160-190-02, 71160-190-04, 71160-190-08, 71160-190-16 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| ALLANTOIN | 344S277G0Z | IACT |
| EDETATE DISODIUM ANHYDROUS | 8NLQ36F6MM | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | 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 |
|---|---|---|---|---|---|---|
| ee8d096c-3bac-e6f9-e053-2995a90ac391 | 6255deae-c3c0-4bc9-b071-843dfef23af7 | 2022-11-28 | Warnings | 6255deae-c3c0-4bc9-b071-843dfef23af7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.