Disney Villains Ursula Hand Sanitizer, Deep Aqua

Manufacturer
Mad Beauty USA LLC
Effective date
2021-12-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:23:49

Label at a glance#

ProductDisney Villains Ursula Hand Sanitizer, Deep Aqua
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Reduces bacteria on hands.

Dosage and administration

Place pea sized drop onto hands. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethylalcohol 69%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Reduces bacteria on hands.

Warnings

WARNINGS SECTION

Flammable. Keep away from source of ignition or flame.

For external use only.

Do not use

OTC - DO NOT USE SECTION

on open skin wound.

When using this product

OTC - WHEN USING SECTION

keep out of eyes.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a doctor immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Place pea sized drop onto hands.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

SPL UNCLASSIFIED SECTION

Store between 15-30°C (59-86°F).

Avoid freezing and excessive heat above 40°C (104°F). 

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua)/Eau, Pentylene Glycol, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Butylene Glycol, Fragrance(Parfum), Sodium Hydroxide, Aloe Barbadensis(Aloe Vera) Leaf Extract.

Questions or Comments

OTC - QUESTIONS SECTION

MAD BEAUTY USA LLC 1030 SALEM ROAD
UNION NJ 07083 MARYLAND
TEL (844) 995 1701

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78789-00178789-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
d2bd1177-f51e-1108-e053-2995a90a55f1a93ccf52-00f1-e114-e053-2995a90ac1ea2021-12-09WarningsExact identifier
spl id: d2bd1177-f51e-1108-e053-2995a90a55f1
spl set id: a93ccf52-00f1-e114-e053-2995a90ac1ea

Reported adverse events (FAERS/openFDA)#

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