Dosage and administration
Apply thoroughly to hands Allow to dry without wiping Do not flush
Travel Safe Hand Sanitizer
- Manufacturer
- Uniters SPA
- Effective date
- 2021-11-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:28:26
Label at a glance#
ProductTravel Safe Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections
Label contents#
Full prescribing information#
Active Ingredient(s)
Benzalkonium Chloride 0.1% v/v. Purpose: Antiseptic
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only.
OTC - WHEN USING SECTION
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or rash develops and continues 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.
Directions
- Apply thoroughly to hands
- Allow to dry without wiping
- Do not flush
Inactive ingredients
Purified water USP, ppg-2 methyl ether, decyl glucoside, c8-10/propylene glycol/peg-22/decylene glycol ether, sodium 2-acrylamido-2-methyl-1-propane sulfonate/sodium acrylate/n-isopropylacrylamide/trimethyl(3-methacrylamidopropyl) ammonium chloride copolymer, citric acid, bronopol, octhilinone
Package Label - Principal Display Panel
8 mL NDC: 77506-005-37 (7.87 in x 8.66 in) (20 cm x 22 cm)
Package label - Principal Display Panel
3.5 mL NDC: 77506-005-00 (7.48 in x 5.31 in) (19 cm x 13.5 cm)
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 77506-005-00 | 2022-09-21 | C162847 | 48780-1 | e4f33bdf-a1a5-d8a0-e053-dadaa90a6e4e | UPP-A MPCC Travel Safe Cloth |
| 77506-005-37 | 2022-09-21 | C162847 | 48780-1 | e4f33bdf-a1a5-d8a0-e053-dadaa90a6e4e | UPP-A MPCC Travel Safe Cloth |
| 77506-005-00 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a1a5-d8a0-e053-dadaa90a6e4e | UPP-A MPCC Travel Safe Cloth |
| 77506-005-37 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a1a5-d8a0-e053-dadaa90a6e4e | UPP-A MPCC Travel Safe Cloth |
Products#
Every source-derived product name is available through these pages.
- Travel Safe Hand Sanitizer
- Benzalkonium Chloride
- PPG-2 METHYL ETHER
- CITRIC ACID MONOHYDRATE
- WATER
- BENZALKONIUM
- DECYL GLUCOSIDE
- SODIUM 2-ACRYLAMIDO-2-METHYL-1-PROPANE SULFONATE/SODIUM ACRYLATE/N-ISOPROPYLACRYLAMIDE/TRIMETHYL(3-METHACRYLAMIDOPROPYL)AMMONIUM CHLORIDE COPOLYMER
- C8-10/PROPYLENE GLYCOL/PEG-22/DECYLENE GLYCOL ETHER
- BRONOPOL
- OCTHILINONE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 77506-005 | 77506-005-00, 77506-005-37 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| e9321e68-31e4-6a16-e053-2995a90a31a1 | a8ebda98-7349-0637-e053-2995a90a0739 | 2022-09-21 | Warnings | a8ebda98-7349-0637-e053-2995a90a0739 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.