Indications and uses
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Mixline
- Manufacturer
- EMPERO LLC | GUANG DONG 3 INS TECHNOLOGY Co.,Ltd
- Effective date
- 2020-04-28
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:08:26
Label at a glance#
ProductMixline
Active ingredientALCOHOL
Label structure10 sections
Dosage and administration
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.
Storage and handling
Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)
Label contents#
Full prescribing information#
Active Ingredient
Alcohol 75% v/v
Purpose
Antiseptic
Uses
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
Flammable. Keep away from heat or flame. For external use only.
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 occurs. These may be signs of a serious condition.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
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 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive ingredients
Alcohol, Water, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Aloe Barbadensis Leaf Juice.
Principal Display Panel
NDC 76778-075-17
Mixline 75% Ethyl Alcohol
Original
INSTANT HAND SANITIZER
- Without soap and water
- Moisturizing formula
- Effective inhibition bacteria
16.9 Fl oz/ 500 ml
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 76778-075-17 | 2021-07-23 | C162847 | 48780-1 | c7ccaba7-12f9-fd44-e053-dadaa90aa01b | 36a8abfe-9145-4a37-8188-5901db2c00a8 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76778-075-17 | Mixline | 500 mL in 1 BOTTLE | SOLUTION | 500 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Mixline
- Alcohol
- WATER
- PROPYLENE GLYCOL
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
- TROLAMINE
- ALOE VERA LEAF
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 76778-075 | 76778-075-17 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) | 59TL3WG5CO | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | 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 |
|---|---|---|---|---|---|---|
| fc5f2b7e-0b6d-4dcf-a0a3-37f261ded373 | 36a8abfe-9145-4a37-8188-5901db2c00a8 | 2020-04-28 | Warnings | fc5f2b7e-0b6d-4dcf-a0a3-37f261ded373 36a8abfe-9145-4a37-8188-5901db2c00a8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.