Dosage and administration
Directions: wet hands thoroughly with product and rubinto skin until dry. Children under 6 years of age should be supervised by an adult when using
HAND SANITIZER
- Manufacturer
- Zhejiang Beta Industry And Trade Co., Ltd.
- Effective date
- 2022-04-12
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-05-31 23:49:10
Label at a glance#
ProductHAND SANITIZER
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(s)
Ethyl Alcohol 75.0%Antimicrobia
Purpose
Antimicrobial
Use
Uses help reduce bacteria on the skin.
Do not use
- in children less than 2 months of age
- on open skin wounds
OTC - WHEN USING SECTION
When using this product avoid contact with face, eyes, and broken skin, In case of eye contact, flush with plenty of water and seek medical advice
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.
Directions
Directions: wet hands thoroughly with product and rubinto skin until dry. Children under 6 years of age should be supervised by an adult when using
Other information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive ingredients
water(aqua), triethanolamine, carbomer, aloealoe barbadensis(aloe vera)leaf juice,fragrance, glycerin, propylene glycol,tocopherol Acetate(Vitamin E)
Package Label - Principal Display Panel
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 77060-101-01 | HAND SANITIZER | 50 mL in 1 BOTTLE | GEL | 50 | 4 | |
| 77060-101-02 | HAND SANITIZER | 60 mL in 1 BOTTLE | GEL | 60 | 4 | |
| 77060-101-03 | HAND SANITIZER | 80 mL in 1 BOTTLE | GEL | 80 | 4 | |
| 77060-101-04 | HAND SANITIZER | 100 mL in 1 BOTTLE | GEL | 100 | 4 | |
| 77060-101-05 | HAND SANITIZER | 150 mL in 1 BOTTLE | GEL | 150 | 4 | |
| 77060-101-06 | HAND SANITIZER | 235 mL in 1 BOTTLE | GEL | 235 | 4 | |
| 77060-101-07 | HAND SANITIZER | 250 mL in 1 BOTTLE | GEL | 250 | 4 | |
| 77060-101-08 | HAND SANITIZER | 300 mL in 1 BOTTLE | GEL | 300 | 4 | |
| 77060-101-09 | HAND SANITIZER | 500 mL in 1 BOTTLE | GEL | 500 | 4 | |
| 77060-101-10 | HAND SANITIZER | 1000 mL in 1 BOTTLE | GEL | 1000 | 4 | |
| 77060-101-11 | HAND SANITIZER | 30 mL in 1 BOTTLE | GEL | 30 | 4 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- HAND SANITIZER
- ALOE VERA LEAF
- WATER
- ALCOHOL
- PROPYLENE GLYCOL
- .ALPHA.-TOCOPHEROL ACETATE, D-
- TROLAMINE
- GLYCERIN
- CARBOMER HOMOPOLYMER TYPE C
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 77060-101 | 77060-101-01, 77060-101-02, 77060-101-03, 77060-101-04, 77060-101-05, 77060-101-06, 77060-101-07, 77060-101-08, 77060-101-09, 77060-101-10, 77060-101-11 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| .ALPHA.-TOCOPHEROL ACETATE, D- | A7E6112E4N | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| CARBOMER HOMOPOLYMER TYPE C | 4Q93RCW27E | 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 |
|---|---|---|---|---|---|---|
| dc71e0b6-145a-0968-e053-2995a90aa4fe | a4838638-b51d-9d6c-e053-2995a90a4ebb | 2022-04-12 | Warnings | dc71e0b6-145a-0968-e053-2995a90aa4fe a4838638-b51d-9d6c-e053-2995a90a4ebb |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.