Indications and uses
to decrease bacteria on the skin that could cause disease recommended for repeated use
Hand Sanitizer
- Manufacturer
- Veritiv Operating Company | Nice-Pak Products, LLC
- Effective date
- 2026-02-16
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 01:46:04
Label at a glance#
ProductHand Sanitizer
Active ingredientALCOHOL
Label structure14 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
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 only
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 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
- for children under 6, use only under adult supervision
- not recommended for infants
Other information
- do not store above 105⁰ 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
Claim
Product is NSF registered for use as a hand sanitizer in and around food processing areas.
Adverse Reaction
Distributed by: Vestis
1035 Alpharetta Street
Suite 2100
Roswell, GA 30075
DSP-TN-21091 DSP-MO-20087
Principal Display Panel
vestis ®
NSF
Nonfood Compounds Program Listed E3 157039
Advanced
Foaming
Hand Sanitizer
70% Alcohol
33.8 FL OZ (1.05 QT) 1 L
DailyMed RxNorm Mappings#
Product Linked Resources#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71897-465-86 | Hand Sanitizer | 1000 mL in 1 BOTTLE, PLASTIC | LIQUID | 1000 | 2 |
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- Alcohol
- WATER
- PEG-8 DIMETHICONE
- GLYCERYL CAPRYLATE/CAPRATE
- ISOPROPYL MYRISTATE
- .ALPHA.-TOCOPHEROL ACETATE
- MEADOWFOAMAMIDOPROPYL BETAINE
- GLYCERIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71897-465 | 71897-465-86 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| PEG-8 DIMETHICONE | GIA7T764OD | IACT |
| GLYCERYL CAPRYLATE/CAPRATE | G7515SW10N | IACT |
| ISOPROPYL MYRISTATE | 0RE8K4LNJS | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| .ALPHA.-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| MEADOWFOAMAMIDOPROPYL BETAINE | HNV0L650LG | IACT |
| GLYCERIN | PDC6A3C0OX | 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 |
|---|---|---|---|---|---|---|
| Hand Sanitizer | ALCOHOL | Veritiv Operating Company | 3b8a41b3-54c5-f5c0-e063-6394a90a9fac | 2026-02-16 | Warnings, Adverse reactions | 71897-465-86 71897-465 71897046586 4af55997-9ad8-7443-e063-6294a90a6c35 3b8a41b3-54c5-f5c0-e063-6394a90a9fac |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.