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.
Advance Hand Sanitizer
- Manufacturer
- Guangzhou Youxing Cosmetics CO.,LTD
- Effective date
- 2020-08-12
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- full-release
- Hydrated at
- 2026-05-31 23:24:34
Label at a glance#
ProductAdvance Hand Sanitizer
Active ingredientALCOHOL
Label structure12 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(s)
Ethyl alcohol 75% V/V
Purpose
Antiseptic
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
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.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
OTC - STOP USE SECTION
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(Aqua). Aloe Barbadensis Leaf Juice,Carbomer, Fragrance. Glycerin,Propylene Glycol ,Tocopheryl Acetate(Vitamin E).Triethanolamine, FD&C Blue No 1. FD&C Yellow No 5
Advance HAnd Sanitizer Refreshing Gel Ethyl Alcohol Antiseptic 75% (240 ml/8 oz)
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75239-005-01 | Advance Hand Sanitizer | 30 mL in 1 BOTTLE | GEL | 30 | 6 | |
| 75239-005-02 | Advance Hand Sanitizer | 50 mL in 1 BOTTLE | GEL | 50 | 6 | |
| 75239-005-03 | Advance Hand Sanitizer | 80 mL in 1 BOTTLE | GEL | 80 | 6 | |
| 75239-005-04 | Advance Hand Sanitizer | 100 mL in 1 BOTTLE | GEL | 100 | 6 | |
| 75239-005-05 | Advance Hand Sanitizer | 120 mL in 1 BOTTLE | GEL | 120 | 6 | |
| 75239-005-06 | Advance Hand Sanitizer | 150 mL in 1 BOTTLE | GEL | 150 | 6 | |
| 75239-005-07 | Advance Hand Sanitizer | 180 mL in 1 BOTTLE | GEL | 180 | 6 | |
| 75239-005-08 | Advance Hand Sanitizer | 200 mL in 1 BOTTLE | GEL | 200 | 6 | |
| 75239-005-09 | Advance Hand Sanitizer | 240 mL in 1 BOTTLE | GEL | 240 | 6 | |
| 75239-005-10 | Advance Hand Sanitizer | 250 mL in 1 BOTTLE | GEL | 250 | 6 | |
| 75239-005-11 | Advance Hand Sanitizer | 300 mL in 1 BOTTLE | GEL | 300 | 6 | |
| 75239-005-12 | Advance Hand Sanitizer | 350 mL in 1 BOTTLE | GEL | 350 | 6 | |
| 75239-005-13 | Advance Hand Sanitizer | 500 mL in 1 BOTTLE | GEL | 500 | 6 | |
| 75239-005-14 | Advance Hand Sanitizer | 650 mL in 1 BOTTLE | GEL | 650 | 6 | |
| 75239-005-15 | Advance Hand Sanitizer | 1000 mL in 1 BOTTLE | GEL | 1000 | 6 | |
| 75239-005-16 | Advance Hand Sanitizer | 3800 mL in 1 BOTTLE | GEL | 3800 | 6 | |
| 75239-005-17 | Advance Hand Sanitizer | 5000 mL in 1 BOTTLE | GEL | 5000 | 6 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Advance Hand Sanitizer
- GLYCERIN
- ALOE VERA LEAF
- FD&C YELLOW NO. 5
- TROLAMINE
- ALPHA-TOCOPHEROL ACETATE
- FD&C BLUE NO. 1
- CARBOMER 934
- PROPYLENE GLYCOL
- BENZYL ALCOHOL
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 75239-005 | 75239-005-01, 75239-005-02, 75239-005-03, 75239-005-04, 75239-005-05, 75239-005-06, 75239-005-07, 75239-005-08, 75239-005-09, 75239-005-10, 75239-005-11, 75239-005-12, 75239-005-13, 75239-005-14, 75239-005-15, 75239-005-16, 75239-005-17 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| FD&C YELLOW NO. 5 | I753WB2F1M | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| ALPHA-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| CARBOMER 934 | Z135WT9208 | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| BENZYL ALCOHOL | LKG8494WBH | IACT |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| acb9a8a4-3c0f-cfb5-e053-2995a90a7b8c | a38e0596-5086-7b23-e053-2995a90a7d9e | 2020-08-12 | Warnings | acb9a8a4-3c0f-cfb5-e053-2995a90a7b8c a38e0596-5086-7b23-e053-2995a90a7d9e |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.