FDA.reportPublic FDA data

Ulta Anti-Bacterial Hand Sanitizer

Manufacturer
Ulta
Effective date
2020-01-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:42:58

Label at a glance#

ProductUlta Anti-Bacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure15 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Alcohol 68%

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Use Decreases bacteria on hands

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with eyes

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness rash develops.

OTHER SAFETY INFORMATION

Flammable: Keep away from flame or high heat.

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 right away.

DOSAGE & ADMINISTRATION SECTION

Directions: Apply sanitizer to hands. Rub hands together until dry.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Aqua (water), Parfum (Fragrance), Isopropyl Alcohol, Glycerin, Carbomer, Aloe Barbadensis Leaf Extract, Triethanolamine, Lactose, Cellulose, Hydroxypropyl Methylcellulose, Benzophenone-4, Retinyl Palmitate, Tocopheryl Acetate, Ultramarine Blue, Yellow 5, Blue 1

OTC - QUESTIONS SECTION

Questions: 1-866-983-8582

SPL UNCLASSIFIED SECTION

Cleanse and condition hands without the use of water.

  • Aloe helps soothe and rejuvenate
  • Vitamins A & E help nourish & protect

SPL UNCLASSIFIED SECTION

NOT TESTED ON ANIMALS

MADE IN CANADA

DISTRIBUTED BY ULTA INC.

BOLINGBROOK, IL 60440

ULTA.COM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ULTAbeauty™

Eucalyptus Mint

HAND SANITIZER GEL

With Aloe, Vitamins A & E

1 fl. oz./29 mL

ULTA eucalyptus mint HSULTA eucalyptus mint HS

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62296-0047-12021-11-30C16284748780-1c7ccaba7-12db-fd44-e053-dadaa90aa01bULTA Eucalyptus Mint Hand Sanitizer
62296-0047-12021-07-23C16284748780-1c7ccaba7-12db-fd44-e053-dadaa90aa01bULTA Eucalyptus Mint Hand Sanitizer

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62296-004762296-0047-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER TYPE C4Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
ANHYDROUS LACTOSE3SY5LH9PMKIACT
ALPHA CELLULOSEI355QGZ19AIACT
HYPROMELLOSES3NXW29V3WOIACT
SULISOBENZONE1W6L629B4KIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB
ULTRAMARINE BLUEI39WR998BIIACT

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
d204f7b5-14e6-a0e3-e053-2a95a90af9c36e8b257c-0652-9de0-e053-2991aa0ad9012021-11-30WarningsExact identifier
spl set id: 6e8b257c-0652-9de0-e053-2991aa0ad901

Reported adverse events (FAERS/openFDA)#

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