Dosage and administration
Wet hands thoroughly with product and allow to dry without wiping. Not recommended for infants; supervise children under 6.
Hand Sanitizer
- Manufacturer
- Mansfield-King, LLC
- Effective date
- 2020-05-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-05-31 23:09:43
Label at a glance#
ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections
Storage and handling
Flammable; keep away from fire or flame.
Label contents#
Full prescribing information#
Active Ingredient(s)
alcohol; 72% w/w
Purpose
Antiseptic; Hand Sanitizer
Use
To decrease bacteria on the skin that could cause disease. Recomended for repeated use.
Warnings
For external use only; hands. Flammable; keep away from fire or flame. When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.
Do not use
Not recommended for infants; supervise children under 6.
OTC - WHEN USING SECTION
When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest. Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wet hands thoroughly with product and allow to dry without wiping. Not recommended for infants; supervise children under 6.
STORAGE AND HANDLING SECTION
Flammable; keep away from fire or flame.
Inactive ingredients
Water (Aqua), Aloe Barbadensis (Aloe Vera) Leaf Juice, Glycerin, Fragrance, Carbomer, Aminomethyl Propanol
Package Label - Principal Display Panel
237 mL. NDC 73827-225-08
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 73827-234-08 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-8b8a-a426-e053-dadaa90af4c2 | Hand sanitizer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73827-234-08 | Hand Sanitizer | 237 mL in 1 BOTTLE | GEL | 237 | 4 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- WATER
- AMINOMETHYLPROPANOL
- GLYCERIN
- CARBOMER INTERPOLYMER TYPE A (55000 CPS)
- ALOE VERA LEAF
- .ALPHA.-TOCOPHEROL ACETATE
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73827-234 | 73827-234-08 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| CARBOMER INTERPOLYMER TYPE A (55000 CPS) | 59TL3WG5CO | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| .ALPHA.-TOCOPHEROL ACETATE | 9E8X80D2L0 | 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 |
|---|---|---|---|---|---|---|
| a4ebaf3b-8800-ac20-e053-2a95a90a1ea5 | a3bc2d91-dedc-abf6-e053-2a95a90a2f24 | 2020-05-05 | Warnings | a4ebaf3b-8800-ac20-e053-2a95a90a1ea5 a3bc2d91-dedc-abf6-e053-2a95a90a2f24 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.