ULTA WHIM

Manufacturer: Carrollclean
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

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

Use

OTC - PURPOSE SECTION

Antiseptic

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Use

INDICATIONS & USAGE SECTION

Decreases bacteria on hands

Warnings

WARNINGS SECTION

For external use only

FLAMMABLE: Keep away from fire or flame.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Extract, Water, Carbomer, Glycerin, Isopropyl Myristate, Phenoxyethanol, Fragrance, Tocopheryl Acetate, Diisopropylamine, FD&C Yellow #5

Dosage

DOSAGE & ADMINISTRATION SECTION

Cleanse and condition hands without the use of water.

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lemon

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	2
581660	ethanol 0.62 ML/ML Topical Gel	SCD	2
581660	ethanol 62 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73708-619-01	2023-01-30	C162847	48780-1	f386c649-a96b-0266-e053-dadaa90a7c1a	ULTA WHIM LEMON HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73708-619-01	ULTA WHIM	29 mL in 1 BOTTLE, DISPENSING	GEL	29		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73708-619	ULTA WHIM (ALCOHOL) GEL [CARROLLCLEAN]	2	Legacy NDC, 1 package rows	20200826_adbac4c5-6f07-8e89-e053-2995a90afd6a.zip

Products#

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

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

ULTA WHIM
ALCOHOL
ISOPROPYL MYRISTATE
PHENOXYETHANOL
ALPHA-TOCOPHEROL ACETATE
DIISOPROPYLAMINE
WATER
ALOE VERA LEAF
GLYCERIN
CARBOMER INTERPOLYMER TYPE A (55000 CPS)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73708-619	73708-619-01

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
ALPHA-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
DIISOPROPYLAMINE	BR9JLI40NO	IACT
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)	59TL3WG5CO	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
adbad8a9-b6f3-57a0-e053-2995a90a5de3			adbac4c5-6f07-8e89-e053-2995a90afd6a	2020-08-25	Warnings	Exact identifier spl id: adbad8a9-b6f3-57a0-e053-2995a90a5de3 spl set id: adbac4c5-6f07-8e89-e053-2995a90afd6a

Reported adverse events (FAERS/openFDA)#

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