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
- Manufacturer
- Sutra Beauty Inc | Guangzhou Joy Claire Biological Technology Co.,Ltd
- Effective date
- 2020-12-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 23:36:05
Label at a glance#
ProductHand Sanitizer
Active ingredientALCOHOL
Label structure13 sections
Storage and handling
Store between 15-30C (59-86F). Avoid freezing and excessive heat above 40C (104F).
Contacts and useful links#
Label contents#
Full prescribing information#
Active Ingredient(s)
Ethyl Alcohol 75% v/v
Inactive ingredients
Aloe Barbadensis Leaf Extract, Aqua, Camellia Sinensis Leaf Oil, Carbomer, Rosmarinus Officinalis (Rosemary) Leaf Oil, Parfum.
Purpose
Antiseptic
Use
Hand Sanitizer to help reduce bacteria that can potentially cause disease. For use when soap and water are not available.
Warnings
For external use only. Flammable, keep away from fire or flame.
Do not use
- On children less than 2 months of age.
- On open skin wounds.
OTC - WHEN USING SECTION
Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
OTC - STOP USE SECTION
Irritation or rash occurs. These may be signs of a serious condition.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).
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).
Questions or Comments?
Call 1-888-463-6332 Monday-Friday 9AM-5PM EST FDA NDC Product Code: 76741-003-12
Package Label - Principal Display Panel
120 ml NDC:76741-003-12
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 76741-003-12 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-677f-a426-e053-dadaa90af4c2 | ad4287fe-2b10-4a40-e053-2995a90a6340 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76741-003-12 | Hand Sanitizer | 120 mL in 1 BOTTLE, DISPENSING | GEL | 120 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- Ethyl Alcohol
- CARBOMER 940
- WATER
- ALCOHOL
- ALOE VERA LEAF
- TEA LEAF OIL
- ROSEMARY OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 76741-003 | 76741-003-12 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CARBOMER 940 | 4Q93RCW27E | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| TEA LEAF OIL | VC855RRT77 | IACT |
| ROSEMARY OIL | 8LGU7VM393 | 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 |
|---|---|---|---|---|---|---|
| b7a21773-cafb-2960-e053-2995a90ada31 | ad4287fe-2b10-4a40-e053-2995a90a6340 | 2020-12-29 | Warnings | b7a21773-cafb-2960-e053-2995a90ada31 ad4287fe-2b10-4a40-e053-2995a90a6340 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.