Indications and uses
Decreases bacieria on skin
Assorted Licensed Hand Sanitizer Vanilla
- Manufacturer
- Shenzhen Lantern Scicence Co.,Ltd. | Shenzhen Lantern Science Co.,Ltd.
- Effective date
- 2024-07-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 00:14:55
Label at a glance#
ProductAssorted Licensed Hand Sanitizer Vanilla 01
Active ingredientALCOHOL
Label structure13 sections
Dosage and administration
Adults and children 6 years and older Spray onto hands and rub together unil dry. Recommended for repeat use. Children under 6 years of age should be supervised when using this product.
Label contents#
Full prescribing information#
Drug Facts
drug facts
Active Ingredient
Active ingredient Purpose
Ethyl Alcohol 70% v/v Antiseptic
Uses
Decreases bacieria on skin
Warning
For external use only
Do not use
lf you are allergic to any of the ingredients
When using this product
Do not get into eyes. lf contact occurs, rinse thoroughly with water.Do not use in or near eyes,In case of eye contact ,flush eyes thoroughly with water. Discontinue if skin becomes irritated and ask for a doctor.
Stop use and ask a doctor
lf irritation or rash develops and continues for more than72 hours.
keep out of reach of children
lf swallowed, get medical help or contact a Poison Control Center immediately.
Directions
Adults and children 6 years and older
Spray onto hands and rub together unil dry. Recommended for repeat use.
Children under 6 years of age
should be supervised when using this product.
Inactive ingredients
Water, Fragrance,Glycerin, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, Aminomethyl Propanol, Tocopheryl Acetate, Aloe Barbadensis Gel, Denatonium Benzoate.
other Information
Storebetween15-30C(59-86F)
Avoid freezing and excessive heat above 40C (104F)
DOSAGE & ADMINISTRATION SECTION
Spray 3-4 times each time.
Used in the skin area of the hands.
packing
packing
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54860-425-01 | Assorted Licensed Hand Sanitizer Vanilla01 | 28 mL in 1 BOTTLE, SPRAY | SPRAY | 28 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Assorted Licensed Hand Sanitizer Vanilla 01
- alcohol
- AMINOMETHYLPROPANOL
- ALOE VERA LEAF
- GLYCERIN
- WATER
- ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)
- .ALPHA.-TOCOPHEROL ACETATE
- DENATONIUM BENZOATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 54860-425 | 54860-425-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) | 8Z5ZAL5H3V | IACT |
| .ALPHA.-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| DENATONIUM BENZOATE | 4YK5Z54AT2 | 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 |
|---|---|---|---|---|---|---|
| Assorted Licensed Hand Sanitizer Vanilla 01 | ALCOHOL | Shenzhen Lantern Scicence Co.,Ltd. | 1cc90b2f-450f-1deb-e063-6394a90a6480 | 2024-07-08 | Warnings | 54860-425-01 54860-425 54860042501 1cc91c34-8d5f-5168-e063-6394a90a6528 1cc90b2f-450f-1deb-e063-6394a90a6480 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.