FDA.reportPublic FDA data

Ultra

Manufacturer
Aldi | Vi-Jon, LLC
Effective date
2022-04-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:04:04

Label at a glance#

ProductUltra
Active ingredientCHLOROXYLENOL
Label structure11 sections

Dosage and administration

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.3%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

 for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only: hands only

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes.  If contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or redness develops
  • 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
  • apply palmful to hands
  • scrub thoroughly
  • rinse thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, sodium C14-16 olefin sulfonate, lauramine oxide and/or lauramidopropylamine oxide and myristamidopropylamine oxide, sodium laureth sulfate, sodium lauryl sulfate, sodium chloride, sodium xylenesulfonate, alcohol denat., fragrance, phenoxyethanol, citric acid, methylisothiazolinone, tetrasodium EDTA, yellow 5, blue 1

SPL UNCLASSIFIED SECTION

WARNING

NOT FOR USE IN DISHWASHERS.

DO NOT ADD BLEACH

Phosphate Free Contains Surfactants

Not tested on animals

ANTIBACTERIAL

HAND SOAP

GREEN APPLE SCENT

Ultra Concentrated

Dishwashing Liquid

DIST. & SOLD EXCLUSIVELY BY:

ALDI, BATAVIA, IL 60510

This product is not manufactured or distributd by Procter & Gamble,  distributor of Dawn Ultra Antibacterial Hand Soap Apple Blossom Scent

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Radiance

TOUCH ON GREASE

ANTIBACTERIAL | HAND SOAP

COMPARE TO DAWN ULTRA ANTIBACTERIAL HAND SOAP APPLE BLOSSOM SCENT

24 FL OZ (710 mL)

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64024-956-502025-02-21C16284748780-12cef2736-5b91-d83d-e063-dadaa90ab31fDrug facts Radiance 956.002/956AE
64024-956-502025-01-30C16284748780-12cef2736-5b91-d83d-e063-dadaa90ab31fDrug facts Radiance 956.002/956AE

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64024-95664024-956-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHLOROXYLENOL0F32U78V2QACTIB
water059QF0KO0RIACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM LAURYL SULFATE368GB5141JIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM XYLENESULFONATEG4LZF950URIACT
ALCOHOL3K9958V90MIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
EDETATE SODIUMMP1J8420LUIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

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
2ea9cbcc-025c-adba-e063-6294a90a88b4be8d31d8-032d-47c2-bad3-4ef993233dbd2025-02-21WarningsExact identifier
spl set id: be8d31d8-032d-47c2-bad3-4ef993233dbd

Reported adverse events (FAERS/openFDA)#

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