Dosage and administration
Pump a small amout into palm rub thoroughly over all surfaces of both hands,rub hands to gether birskly until dry.
antibacterial hand sanitizer
- Manufacturer
- Yuyao Jessie Commodity Co.,Ltd.
- Effective date
- 2022-12-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:44:05
Label at a glance#
Productantibacterial hand sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections
Label contents#
Full prescribing information#
Active Ingredient
Benzalkonium chloride 0.4%
Purpose
Antibacterial
Use
for hand washing to decrease bacteria on skin
WARNINGS
For External use only-hands.
When using this produt.avoid contact with eyes.In case of eye contact ,flush eyes with water.
Stop use and ask a doctor.if irritation or redness develops,or if condition persists for more than 72 hours.
keep out of reach of children if swallowed,get medical help to contact a poison control center reght away
keep out of reach of children unless under adult supervision .if seallowed ,get medical help or contact a Poison Control Center immediately.
Directions
Pump a small amout into palm
rub thoroughly over all surfaces of both hands,rub hands to gether birskly until dry.
Inactive ingredients
Deionizer Water, Glycerin, Silicone oil, Aloe Barbadensis Leaf Extrac, Propylene glycol, Kathon, EDTA-2NA, Tocopherol Acetate
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- antibacterial hand sanitizer
- Benzalkonium Chloride
- WATER
- GLYCERIN
- ALOE VERA FLOWER
- EDETIC ACID
- SILICON
- PROPYLENE GLYCOL BEHENATE
- BENZALKONIUM
- ALPHA-TOCOPHEROL ACETATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51414-103 | 51414-103-01, 51414-103-02, 51414-103-03, 51414-103-04, 51414-103-05, 51414-103-06, 51414-103-07, 51414-103-08, 51414-103-09, 51414-103-10, 51414-103-11, 51414-103-12, 51414-103-13, 51414-103-14, 51414-103-15, 51414-103-16, 51414-103-17, 51414-103-18, 51414-103-19, 51414-103-20, 51414-103-21, 51414-103-22, 51414-103-23, 51414-103-24 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| ALOE VERA FLOWER | 575DY8C1ER | IACT |
| EDETIC ACID | 9G34HU7RV0 | IACT |
| SILICON | Z4152N8IUI | IACT |
| PROPYLENE GLYCOL BEHENATE | Z101D9Y62T | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| ALPHA-TOCOPHEROL ACETATE | 9E8X80D2L0 | 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 |
|---|---|---|---|---|---|---|
| f0033086-4ab3-b3e3-e053-2995a90ad171 | 41f7e33d-30a1-5d2d-e054-00144ff8d46c | 2022-12-17 | Warnings | f0033086-4ab3-b3e3-e053-2995a90ad171 41f7e33d-30a1-5d2d-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.