Dosage and administration
For occasional and personal domestic use, spray on the palm of hands and rub together for 30 seconds. Allow to dry. Supervise children when they use this product.
Hand Sanitizer
- Manufacturer
- Sanihealth Labs Inc.
- Effective date
- 2021-09-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:42:23
Label at a glance#
ProductHand 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 70% v/v. Purpose: Antiseptic
Purpose
Antiseptic, Hand Sanitizer
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
- For occasional and personal domestic use, spray on the palm of hands and rub together for 30 seconds. Allow to dry. Supervise children when they use this product.
Other information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive ingredients
Water, glycerol, hydrolyzed jojoba esters, fragrance, tocopheryl acetate, denatonium benzoate
Package Label - Principal Display Panel
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 79861-003-38 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a99e-d8a0-e053-dadaa90a6e4e | Jack Wylde Hand sanitizer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79861-003-38 | Hand Sanitizer | 38 mL in 1 BOTTLE | GEL | 38 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- ALCOHOL
- GLYCERIN
- HYDROLYZED JOJOBA ESTERS (ACID FORM)
- WATER
- .ALPHA.-TOCOPHEROL ACETATE
- DENATONIUM BENZOATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 79861-003 | 79861-003-38 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| HYDROLYZED JOJOBA ESTERS (ACID FORM) | UDR641JW8W | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| .ALPHA.-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| DENATONIUM BENZOATE | 4YK5Z54AT2 | 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 |
|---|---|---|---|---|---|---|
| cbe404fb-85e0-eee4-e053-2995a90a068d | cbe2cd63-a47a-0588-e053-2995a90a0a23 | 2021-09-13 | Warnings | cbe404fb-85e0-eee4-e053-2995a90a068d cbe2cd63-a47a-0588-e053-2995a90a0a23 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.