Hand Sanitizer

Manufacturer
Uline | Nice-Pak Products, LLC
Effective date
2026-02-17
Label type
HUMAN OTC DRUG LABEL
Version
16
Source
full-release
Hydrated at
2026-06-01 01:46:04

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommend for repeated use

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

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease
  • recommend for repeated use

Warnings

WARNINGS SECTION

For external use only: hands

Flammable, keep away from fire and flame.

When using this product

OTC - WHEN USING SECTION

  • 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

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

OTHER SAFETY INFORMATION

  • do not store above 105⁰F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, carbomer or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

Adverse event

ADVERSE REACTIONS SECTION

*Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

Distributed by: ULINE

12575 Uline Drive, Pleasant Prairie, WI 53158

1-800-295-5510 - uline.com

Pat. 9,161,982

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENRICHED WITH MOISTURIZERS

ULINE

Hand Sanitizer

Kills more than 99.99% of germs*

S-21262

2 FL OZ (59 mL)

image descriptionimage description

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN16
581662ethanol 0.7 ML/ML Topical GelSCD16
581662ethanol 70 % Topical GelSY16
581662ethyl alcohol 70 % Topical GelSY16

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69790-770-16Hand Sanitizer59 mL in 1 BOTTLE, PLASTICGEL5916
69790-770-34Hand Sanitizer236 mL in 1 BOTTLE, PLASTICGEL23616
69790-770-88Hand Sanitizer1999 mL in 1 BOTTLE, PLASTICGEL199916
69790-770-96Hand Sanitizer221 mL in 1 BOTTLE, PUMPGEL22116

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69790-77069790-770-16, 69790-770-96, 69790-770-34, 69790-770-88

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML · Source PDF

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hand SanitizerETHYL ALCOHOLUline3bc9cfa2-2b1f-4892-93ff-cffa9f5878042026-02-17Warnings, Adverse reactionsExact identifier
ndc (package): 69790-770-16
ndc (package): 69790-770-88
ndc (package): 69790-770-96
ndc (package): 69790-770-34
ndc (product): 69790-770
ndc11 (package): 69790077088
ndc11 (package): 69790077096
ndc11 (package): 69790077016
ndc11 (package): 69790077034
spl id: 4b09908e-c64c-c362-e063-6294a90ab66d
spl set id: 3bc9cfa2-2b1f-4892-93ff-cffa9f587804

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.