FDA.reportPublic FDA data

Alcohol

Manufacturer
Uline | Nice-Pak Products, LLC
Effective date
2026-02-17
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:46:19

Label at a glance#

ProductAlcohol
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended 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 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For exterenal use only: hands

Flammable, keep away from fire or 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

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, carbomer and/or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, glycerin, isopropyl myristate, tocopheryl acetate

ADVERSE REACTION

ADVERSE REACTIONS SECTION

Distributed by: ULINE

12575 Uline Drive, Pleasant Prairie, WI 53158

1-800-295-5510  uline.com

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

SDS-MO-15036 DSP-MO-34 SDS-TN-15012 DSP-TN-15000 DSP-MO-28

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENRICHED WITH MOISTURIZERS

ULINE

Hand Sanitizer

Kills 99.99% of germs*

S-23797

1 GALLON (3.79 L)

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69790-849-082022-08-26C16284748780-1e4f33bdf-af39-d8a0-e053-dadaa90a6e4eUline 849.001/849BA Moisturizing Hand Sanitizer
69790-849-552022-08-26C16284748780-1e4f33bdf-af39-d8a0-e053-dadaa90a6e4eUline 849.001/849BA Moisturizing Hand Sanitizer
69790-849-682022-08-26C16284748780-1e4f33bdf-af39-d8a0-e053-dadaa90a6e4eUline 849.001/849BA Moisturizing Hand Sanitizer
69790-849-082022-07-29C16284748780-1e4f33bdf-af39-d8a0-e053-dadaa90a6e4eUline 849.001/849BA Moisturizing Hand Sanitizer
69790-849-552022-07-29C16284748780-1e4f33bdf-af39-d8a0-e053-dadaa90a6e4eUline 849.001/849BA Moisturizing Hand Sanitizer
69790-849-682022-07-29C16284748780-1e4f33bdf-af39-d8a0-e053-dadaa90a6e4eUline 849.001/849BA Moisturizing Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69790-849-08Alcohol3785 mL in 1 BOTTLE, PLASTICLIQUID37859
69790-849-55Alcohol2082 mL in 1 DRUMLIQUID20829
69790-849-68Alcohol2000 mL in 1 BOTTLE, PLASTICLIQUID20009

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69790-84969790-849-68, 69790-849-08, 69790-849-55

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
TOCOPHEROLR0ZB2556P8IACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

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
AlcoholALCOHOLUlinefdda41fa-d847-4cee-a070-91f0600b0fc82026-02-17Warnings, Adverse reactionsExact identifier
ndc (package): 69790-849-68
ndc (package): 69790-849-55
ndc (package): 69790-849-08
ndc (product): 69790-849
ndc11 (package): 69790084908
ndc11 (package): 69790084955
ndc11 (package): 69790084968
spl id: 4b09a991-ce1b-ead1-e063-6294a90afce2
spl set id: fdda41fa-d847-4cee-a070-91f0600b0fc8

Reported adverse events (FAERS/openFDA)#

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