Derma Intensive Hand Sanitizer

Manufacturer: Rubella Beauty AD
Effective date: 2020-05-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:29:04

Label at a glance#

ProductDerma Intensive Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 65%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on skin
Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire or flame

When using this product

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, rinse thoroughly with water

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develops and persists for more than 48 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

6 year olds and younger should only use under supervision of adults. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping

Other information

SPL UNCLASSIFIED SECTION

Store below 105°F/40.5°C
May discolor fabrics or sfacures

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Acrylates/c10-30 Alkyl Acrylate crosspolymer, Glycerin, Parfum (Fragrance), Triethanolamine, Menthol, Linalool

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Derma Intensive Hand Sanitizer
ALCOHOL
WATER
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
GLYCERIN
TROLAMINE
MENTHOL
LINALOOL, (+/-)-

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65445-000	65445-000-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
GLYCERIN	PDC6A3C0OX	IACT
TROLAMINE	9O3K93S3TK	IACT
MENTHOL	L7T10EIP3A	IACT
LINALOOL, (+/-)-	D81QY6I88E	IACT
ALCOHOL	3K9958V90M	ACTIB

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
cd89cd8e-75fa-7824-e053-2a95a90aa108			a68fb91f-4f51-76bd-e053-2a95a90a057f	2021-10-04	Warnings	Exact identifier spl set id: a68fb91f-4f51-76bd-e053-2a95a90a057f

Reported adverse events (FAERS/openFDA)#

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