Storage and handling
Other information do not store above 105°F may discolor some fabics harmful to wood finished and plastics
Hand Sanitizer
- Manufacturer
- Ultra Distributors Inc.
- Effective date
- 2020-06-03
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:15:56
Label at a glance#
ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient
Ethyl Alcohol 70%
OTC - PURPOSE SECTION
Purpose
Antiseptic
INDICATIONS & USAGE SECTION
Uses to decrease bacteria on the skin that could cause disease recommended for repeated use
WARNINGS SECTION
Warnings
for external use only: hands
Flammable. Keep away from fire or flame
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.
OTC - STOP USE SECTION
Stop use and ask a doctor if . irritation or redness develops. condition persists for more than 72 hours
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(1-800-222-1222)right away .
DOSAGE & ADMINISTRATION SECTION
Directions
- wet hands thoroughly with product and allow to dry without wiping.
- for children under 6 , use only under adult supervision.
- not recommented for infants .
STORAGE AND HANDLING SECTION
Other information
- do not store above 105°F
- may discolor some fabics
- harmful to wood finished and plastics
INACTIVE INGREDIENT SECTION
Inactive ingredients
acrylates/C10-C30 alkyl acrylate crosspolymer,aloe barbadensis leaf juice, aminomethyl propanol, glycerin, maltodextrin, propylene glycol, water , tocopheryl acetate
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 78495-008-01 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-7059-d83d-e063-dadaa90ab31f | a72843fc-0efa-5fa0-e053-2a95a90a6416 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 78495-008-01 | Hand Sanitizer | 236 mL in 1 BOTTLE, PUMP | GEL | 236 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- ETHYL ALCOHOL
- MALTODEXTRIN
- PROPYLENE GLYCOL
- WATER
- ALOE VERA LEAF
- GLYCERIN
- CARBOMER INTERPOLYMER TYPE A (55000 CPS)
- .ALPHA.-TOCOPHEROL ACETATE
- ALCOHOL
- AMINOMETHYLPROPANOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 78495-008 | 78495-008-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| WATER | 059QF0KO0R | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| CARBOMER INTERPOLYMER TYPE A (55000 CPS) | 59TL3WG5CO | IACT |
| .ALPHA.-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| AMINOMETHYLPROPANOL | LU49E6626Q | 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 |
|---|---|---|---|---|---|---|
| a72843fc-0efb-5fa0-e053-2a95a90a6416 | a72843fc-0efa-5fa0-e053-2a95a90a6416 | 2020-06-03 | Warnings | a72843fc-0efb-5fa0-e053-2a95a90a6416 a72843fc-0efa-5fa0-e053-2a95a90a6416 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.