Dosage and administration
Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children under 6 years of ages should be supervised when using this product.
Hand Sanitizer
- Manufacturer
- Dongyang Mukang Pharmaceutical Factory
- Effective date
- 2020-11-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:33:39
Label at a glance#
ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections
Storage and handling
Do not store above 110℉（40℃） May discolor certain fabrics or surfaces
Label contents#
Full prescribing information#
Active Ingredient(s)
Alcohol 70% v/v. Purpose: Antiseptic
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria on the skin that could cause disease.
Recommended for repeated use.
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 do not use in or near the eyes. In case of contact , rinse eyes thoroughly with water.
- Avoid contact with broken skin
- Do not inhale or ingest.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or rash oppears and lasts.
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 in your palm to thoroughly cover your hands
- Rub hands together briskly until dry
- Children under 6 years of ages should be supervised when using this product.
Other information
- Do not store above 110℉（40℃）
- May discolor certain fabrics or surfaces
Inactive ingredients
Water, Carbomer, AMP-95 aminomethly propanol, jasmine scent, aloe vera, FD&C yellow no.5(tartrazine), and FD&C blue no.1
Package Label - Principal Display Panel
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 75586-010-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-65b2-a426-e053-dadaa90af4c2 | 75586-010-01 3780ml |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75586-010-01 | Hand Sanitizer | 3780 mL in 1 BOTTLE | GEL | 3780 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- ALCOHOL
- ALOE VERA LEAF
- FD&C BLUE NO. 1
- FD&C YELLOW NO. 5
- AMINOMETHYLPROPANOL
- JASMINUM OFFICINALE LEAF
- WATER
- CARBOMER COPOLYMER TYPE A
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 75586-010 | 75586-010-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| FD&C YELLOW NO. 5 | I753WB2F1M | IACT |
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| JASMINUM OFFICINALE LEAF | 6OG06384ID | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| CARBOMER COPOLYMER TYPE A | 71DD5V995L | 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 |
|---|---|---|---|---|---|---|
| b3f77ea9-fa53-bcc1-e053-2995a90a032a | b3f77ea9-fa64-bcc1-e053-2995a90a032a | 2020-11-13 | Warnings | b3f77ea9-fa53-bcc1-e053-2995a90a032a b3f77ea9-fa64-bcc1-e053-2995a90a032a |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.