Ulta WHIM Peach

Manufacturer
CarrollClean LLC
Effective date
2020-08-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:25:49

Label at a glance#

ProductUlta WHIM Peach
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Cleanse and condition hands without the use of water.

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

Cleanse and condition hands without the use of water.

Active

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Decreases bacteria on hands

Warnings

WARNINGS SECTION

For external use only

FLAMMABLE Keep away from fire or flame.

Inactive

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Extract, Water, Carbomer, Glycerin, Isoproypl Myristate, Phenoxyethanol, Fragrance, Tocophenyl Acetate, Diisopropylamine, FD&C Yellow #6, FD&C Red #40.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PeachPeach

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73708-622-012023-01-30C16284748780-1f386c649-c72b-0266-e053-dadaa90a7c1aUlta WHIM Peach

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73708-622-01Ulta WHIM Peach29 mL in 1 BOTTLE, DISPENSINGGEL292

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73708-622ULTA WHIM PEACH (ALCOHOL) GEL [CARROLLCLEAN LLC]2Legacy NDC, 1 package rows20200826_adbb4889-5f6e-a0d5-e053-2a95a90a693f.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73708-62273708-622-01

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

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
adbb4889-5f6f-a0d5-e053-2a95a90a693fadbb4889-5f6e-a0d5-e053-2a95a90a693f2020-08-25WarningsExact identifier
spl id: adbb4889-5f6f-a0d5-e053-2a95a90a693f
spl set id: adbb4889-5f6e-a0d5-e053-2a95a90a693f

Reported adverse events (FAERS/openFDA)#

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