ULTA WHIM CUPCAKE

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 CUPCAKE

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

Cleanse and condition hands without the use of water.

Label contents#

Full prescribing information#

Active

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Directions

DOSAGE & ADMINISTRATION SECTION

Cleanse and condition hands without the use of water.

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, Isopropyl Myristate, Phenoxyethanol, Fragrance, Tocopheryl Acetate, Diisopropylamine, D&C Violet #2, D&C Red #33

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cupcake

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
73708-620-29	2023-01-30	C162847	48780-1	f386c64a-1c17-0266-e053-dadaa90a7c1a	ULTA WHIM CUPCAKE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73708-620-29	ULTA WHIM CUPCAKE	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
73708-620	ULTA WHIM CUPCAKE (ALCOHOL) GEL [CARROLLCLEAN LLC]	2	Legacy NDC, 1 package rows	20200826_adbb4082-8369-4378-e053-2995a90ab54f.zip

Products#

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

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73708-620	73708-620-29

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
DIISOPROPYLAMINE	BR9JLI40NO	IACT
WATER	059QF0KO0R	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALCOHOL	3K9958V90M	ACTIB
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)	59TL3WG5CO	IACT
GLYCERIN	PDC6A3C0OX	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	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
adbb4889-5f65-a0d5-e053-2a95a90a693f			adbb4082-8369-4378-e053-2995a90ab54f	2020-08-25	Warnings	Exact identifier spl id: adbb4889-5f65-a0d5-e053-2a95a90a693f spl set id: adbb4082-8369-4378-e053-2995a90ab54f

Reported adverse events (FAERS/openFDA)#

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