Derma-San

Manufacturer
Anderson Chemical Company
Effective date
2020-05-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:45

Label at a glance#

ProductDerma-San
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Pump a small amounts of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chlorine, 0.1% w/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on skin
  • Recommended for repeated use

Warning

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes.
  • in case on eye contact, flush eyes with water

Use

RECENT MAJOR CHANGES SECTION

  • For handwashing to decrease bacteria on skin.
  • Recommended for repeated use.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or redness develops or if condition persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump a small amounts of foam into palm of hand.
  • Rub thoroughly over all surfaces of both hands.
  • Rub hands together briskly until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, cetrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, and citric acid.

Questions or comment?

OTC - QUESTIONS SECTION

320-693-2477

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Derma-San

NO-RINSE HAND SANITIZER

NET CONTENTS: 1 US GALLON

ProductLabelProductLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038791benzalkonium chloride 0.1 % Topical SolutionPSN1
1038791benzalkonium chloride 1 MG/ML Topical SolutionSCD1
1038791benzalkonium chloride 0.1 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63131-0006-12022-01-28C16284748780-1d6a99b39-8bb4-a426-e053-dadaa90af4c2a49c41fd-e31d-b451-e053-2995a90a0dc6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63131-0006-1Derma-San3785 mL in 1 JUGLIQUID37851
63131-0006-1Derma-San7570 in 1 CASELIQUID75701

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63131-0006DERMA-SAN (BENZALKONIUM CHLORIDE) LIQUID [ANDERSON CHEMICAL COMPANY]1Legacy NDC, 2 package rows20200506_a49c41fd-e31d-b451-e053-2995a90a0dc6.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63131-000663131-0006-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML · Source PDF

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
a49c41fd-e31e-b451-e053-2995a90a0dc6a49c41fd-e31d-b451-e053-2995a90a0dc62020-05-01WarningsExact identifier
spl id: a49c41fd-e31e-b451-e053-2995a90a0dc6
spl set id: a49c41fd-e31d-b451-e053-2995a90a0dc6