Dosage and administration
Directions ●Place enough product on hands to cover all surfaces. Rub hands together until dry. ●Supervise children under 6 years of age when using this product to avoid swallowing.
Hand Sanitizer
- Manufacturer
- NINGBO MEITELI COSMETICS CO., LTD
- Effective date
- 2024-09-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 00:19:48
Label at a glance#
ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections
Storage and handling
●Store, between 15-30 °C (59-86 °F) ●Avoid freezing and excessive heat above 40°C (104°F)
Label contents#
Full prescribing information#
Active Ingredient(s)
ETHYL ALCOHOL 75%
Purpose
Antiseptic
Use
Use Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap
and water are not available.
Warnings
Warnings For external use only. Flammable. Keep away from heat or flame.
Do not use
Do not use on open skin wounds. in children less than 2 months of age.
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.
OTC - STOP USE SECTION
Stop use Stop use and ask a doctor if iritation or rash occurs. These may be signs of a serious condition.
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
Directions
●Place enough product on hands to cover all surfaces. Rub hands together until dry.
●Supervise children under 6 years of age when using this product to avoid swallowing.
Other information
●Store, between 15-30 °C (59-86 °F)
●Avoid freezing and excessive heat above 40°C (104°F)
Inactive ingredients
Water (Aqua), Butylene Glycol, Tocopheryl Acetate Aloe Barbadensis Leaf Extract
Package Label - Principal Display Panel
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 75541-014-01 | 2026-01-29 | C162847 | 48780-1 | 49896155-b35d-586f-e063-e6dba90add90 | 75541-014 |
| 75541-014-02 | 2026-01-29 | C162847 | 48780-1 | 49896155-b35d-586f-e063-e6dba90add90 | 75541-014 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75541-014-01 | Hand Sanitizer | 10 mL in 1 BOTTLE | LIQUID | 10 | 1 | |
| 75541-014-02 | Hand Sanitizer | 20 mL in 1 BOTTLE | LIQUID | 20 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- ALPHA-TOCOPHEROL ACETATE
- ALOE VERA LEAF
- WATER
- BUTYLENE GLYCOL
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 75541-014 | 75541-014-01, 75541-014-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALPHA-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| WATER | 059QF0KO0R | IACT |
| BUTYLENE GLYCOL | 3XUS85K0RA | 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 |
|---|---|---|---|---|---|---|
| 22611887-106a-81b3-e063-6394a90a707e | 2260fd39-0e71-b451-e063-6394a90ac2c3 | 2024-09-13 | Warnings | 22611887-106a-81b3-e063-6394a90a707e 2260fd39-0e71-b451-e063-6394a90ac2c3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.