Indications and uses
to decrease bacteria on the skin that could cause disease recommended for repeated use
HAND SANITIZER
- Manufacturer
- Ultra Distributors Inc
- Effective date
- 2020-09-04
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:28:31
Label at a glance#
ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure11 sections
Dosage and administration
wet hands thoroughly with product and allow to dry without wiping. for children under 6 , use only under adult supervision. not recommended for infants .
Storage and handling
do not store above 105°F may discolor some fabics harmful to wood finished and plastics
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient
Ethyl Alcohol 62%
Purpose
Antiseptic
Uses
- to decrease bacteria on the skin that could cause disease
- recommended 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.
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.
Directions
- wet hands thoroughly with product and allow to dry without wiping.
- for children under 6 , use only under adult supervision.
- not recommended for infants .
Other information
- do not store above 105°F
- may discolor some fabics
- harmful to wood finished and plastics
Inactive ingredients
water, glycerin, propylene glycol, acrylates/C10-C30 alkyl acrylate crosspolymer, triethanolamine, aloe barbadensis leaf juice, maltodextrin
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 78495-002-01 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-603e-d83d-e063-dadaa90ab31f | HAND SANITIZER Cars |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 78495-002-01 | HAND SANITIZER | 59 mL in 1 BOTTLE, PLASTIC | GEL | 59 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- HAND SANITIZER
- ETHYL ALCOHOL
- MALTODEXTRIN
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)
- ALCOHOL
- ALOE VERA LEAF
- TROLAMINE
- WATER
- GLYCERIN
- PROPYLENE GLYCOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 78495-002 | 78495-002-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) | 71DD5V995L | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | 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 |
|---|---|---|---|---|---|---|
| ae878ac6-3f68-ce74-e053-2995a90a0700 | ae87b3d1-b854-acf5-e053-2a95a90a89d0 | 2020-09-04 | Warnings | ae878ac6-3f68-ce74-e053-2995a90a0700 ae87b3d1-b854-acf5-e053-2a95a90a89d0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.