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.
Hand Sanitizer Advance
- Manufacturer
- Comercializadora Mca, S.A. de C.V.
- Effective date
- 2020-10-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:31:14
Label at a glance#
ProductHand Sanitizer Advance
Active ingredientALCOHOL
Label structure11 sections
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 70% v/v.
Purpose
Antiseptic
Use
Health care personnel hand rub to help reduce bacteria that potentially can cause disease.
Warnings
For external use only. Flammable. Keep away from heat or flame.
Do not use
- in children less than 2 months of age
- on open skin wounds
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 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
- 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
Water, carboner, triethanolamine, glycerine, propylene glycol, fragrance, aloe barbadensis leaf juice.
Made in Mexico by COMERCIALIZADORA MCA SA DE CV, LEON, GTO, MEXICO.
Questions? salesmx@besser-chem.com
Package Label - Principal Display Panel
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 80717-001-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-96a9-a426-e053-dadaa90af4c2 | 8e7eac95-c7ff-48d6-8861-e7ddcff34341 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80717-001-01 | Hand Sanitizer Advance | 1000 mL in 1 BOTTLE, PLASTIC | GEL | 1000 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer Advance
- Alcohol
- WATER
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
- GLYCERIN
- BACKHOUSIA CITRIODORA LEAF OIL
- ALOE VERA LEAF
- PROPYLENE GLYCOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 80717-001 | 80717-001-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
| CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE | 0A5MM307FC | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| BACKHOUSIA CITRIODORA LEAF OIL | 2UQQ0PI06P | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | 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 |
|---|---|---|---|---|---|---|
| 66bb3e8e-65ab-4cba-a360-e6543caafeab | 8e7eac95-c7ff-48d6-8861-e7ddcff34341 | 2020-10-08 | Warnings | 66bb3e8e-65ab-4cba-a360-e6543caafeab 8e7eac95-c7ff-48d6-8861-e7ddcff34341 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.