DERMACEN FOAMING INSTANT HAND SANITIZER WITH ALOE

Manufacturer
Central Solutions Inc
Effective date
2024-12-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:41:31

Label at a glance#

ProductDERMACEN FOAMING INSTANT HAND SANITIZER WITH ALOE
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

An effective antimicrobial hand cleanser for topical application Recommended for repeated use Reduces transient microorganisms on intact skin Keeps hands from drying out due to repeated uses

Dosage and administration

Wet hands thoroughly with product. Allow to dry without wiping. Use no water or towels

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • An effective antimicrobial hand cleanser for topical application
  • Recommended for repeated use
  • Reduces transient microorganisms on intact skin
  • Keeps hands from drying out due to repeated uses

Warnings

WARNINGS SECTION

  • For External Use Only
  • Flammable, keep away from fire or open flame

OTC - WHEN USING SECTION

When using this product:

  • Avoid contact with eyes
  • In case of eye contact, flush with water for 15 minutes

OTC - DO NOT USE SECTION

  • Discontinue use and see a doctor if irritation occurs
  • Avoid contact with broken skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product. Allow to dry without wiping. Use no water or towels

Other information

OTHER SAFETY INFORMATION

Not tested on animals

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, PEG-10 Acrylate/Perfluorohexylethyl Acrylate Compolymer/Perfluorohexyethyl Alcohol, Glycereth 26, Citric Acid, Fragrance, Aloe Barbadensis Leaf Juice

Questions?

OTC - QUESTIONS SECTION

Call 800-255-0262

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DermaCen

Foaming

Instant Hand

Sanitizer

with Aloe

For hand washing

to decrease bacteria

on the skin

Net Contents

8.5 oz (251 mL)

container labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN2
616805ethanol 0.7 ML/ML Topical FoamSCD2
616805ethanol 70 % Topical FoamSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62654-149-13DERMACEN FOAMING INSTANT HAND SANITIZER WITH ALOE1000 mL in 1 BOTTLESOLUTION10002
62654-149-14DERMACEN FOAMING INSTANT HAND SANITIZER WITH ALOE251 mL in 1 BOTTLESOLUTION2512

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62654-149DERMACEN FOAMING INSTANT HAND SANITIZER WITH ALOE (ALCOHOL) SOLUTION [CENTRAL SOLUTIONS INC]2Current NDC, Legacy NDC, 2 package rows20241210_d56b9930-b8b0-ad72-e053-2a95a90af590.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62654-14962654-149-14, 62654-149-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
DERMACEN FOAMING INSTANT HAND SANITIZER WITH ALOEALCOHOLCentral Solutions Incd56b9930-b8b0-ad72-e053-2a95a90af5902024-12-09WarningsExact identifier
ndc (package): 62654-149-14
ndc (package): 62654-149-13
ndc (product): 62654-149
ndc11 (package): 62654014913
ndc11 (package): 62654014914
spl id: 28da8c6c-b9e8-e350-e063-6294a90aa108
spl set id: d56b9930-b8b0-ad72-e053-2a95a90af590

Reported adverse events (FAERS/openFDA)#

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