Indications and uses
to decrease bacteria on the skin that could cause disease recommended for repeated use
Hand Sanitizer
- Manufacturer
- Uline | Nice-Pak Products, LLC
- Effective date
- 2026-02-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 11
- Source
- full-release
- Hydrated at
- 2026-06-01 01:46:11
Label at a glance#
ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 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
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient
Ethyl alcohol 70%
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
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach 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
- for children under 6, use only under adult supervision
- not recommended for infants
Other information
- do not store above 105° F
- may discolor some fabrics
- harmful to wood finishes and plastics
Inactive ingredients
water, PEG-8 Dimethicone, meadowfoamamidopropyl betaine, glyceryl caprylate/caprate, glycerin, tocopheryl acetate, isopropyl Myristate
ADVERSE REACTION
*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.
Distributed by: ULINE
12575 Uline Drive, Pleasant Prairied, WI 53158
1-800-295-5510 uline.com
DSP-TN-21091 DSP-MO-20087 DSP-MO-28 SDS-MO-20068
principal display panel
ULINE
Foaming
Hand Samitizer
Kills 99.99% of germs instantly*
S-24121
18 FL OZ (532 mL)
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69790-456-44 | Hand Sanitizer | 532 mL in 1 BOTTLE, PLASTIC | LIQUID | 532 | 11 |
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- Alcohol
- WATER
- PEG-8 DIMETHICONE
- MEADOWFOAMAMIDOPROPYL BETAINE
- GLYCERYL CAPRYLATE/CAPRATE
- GLYCERIN
- .ALPHA.-TOCOPHEROL ACETATE
- ISOPROPYL MYRISTATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69790-456 | 69790-456-44 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| PEG-8 DIMETHICONE | GIA7T764OD | IACT |
| MEADOWFOAMAMIDOPROPYL BETAINE | HNV0L650LG | IACT |
| GLYCERYL CAPRYLATE/CAPRATE | G7515SW10N | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| .ALPHA.-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| ISOPROPYL MYRISTATE | 0RE8K4LNJS | 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 |
|---|---|---|---|---|---|---|
| Hand Sanitizer | ALCOHOL | Uline | 8ed759a2-fb0e-474e-8245-ddb798e542ff | 2026-02-17 | Warnings, Adverse reactions | 69790-456-44 69790-456 69790045644 4b096c45-e6ae-850c-e063-6294a90abd9a 8ed759a2-fb0e-474e-8245-ddb798e542ff |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.