AMERIDERM

Manufacturer
SHIELD LINE LLC
Effective date
2025-11-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:17:46

Label at a glance#

ProductAMERIDERM
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

• for hand washing to decrease bacteria on the skin • recommended for repeated use • for body wash to help reduce bacteria that can potentially cause disease

Dosage and administration

• Apply to hands and wet as needed, vigorously work into a lather and rinse thoroughly

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride...0.10% w/w

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

• for hand washing to decrease bacteria on the skin • recommended for repeated use
• for body wash to help reduce bacteria that can potentially cause disease

Warnings

WARNINGS SECTION

​ For external use only

When using this product

OTC - WHEN USING SECTION

• Avoid contact with eyes, in case of eye contact flush with water

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develops

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply to hands and wet as needed, vigorously
work into a lather and rinse thoroughly

Other information

OTHER SAFETY INFORMATION

Store in a cool dry place below 104 F°

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Triethanolamine Lauryl Sulfate,
Cocamidopropyl Betaine (CAPD), Cocamide MEA,
Polyquaternium 7, Sodium Chloride, Glyceryl Distearate,

Sodium Benzoate, PEG-7 Glyceryl
Cocoate, Fragrance, Sodium C14-15 Olefin Sulfonate,

Methylchloroisothiazolinone and
Methylisothiazolinone, Aloe Barbadensis Gel,
Butyrospermum Parkii (Shea Butter), Citric Acid,
D&C RED # 33, D&C YELLOW # 10

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DRUG FACT PANELDRUG FACT PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1665365benzalkonium chloride 0.1 % Medicated ShampooPSN1
1665365benzalkonium chloride 1 MG/ML Medicated ShampooSCD1
1665365benzalkonium chloride 0.1 % Medicated ShampooSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130352410805455GTIN-13: 0352410805455
EAN-13: 0352410805455
GTIN-12: 352410805455
UPC-A: 352410805455
GTIN storage (14 digits): 00352410805455
ALL-272 AmeriSilk Labels.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52410-8054-5AMERIDERM237 g in 1 BOTTLESHAMPOO2371

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52410-805452410-8054-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
AMERIDERMBZKSHIELD LINE LLC440b711a-de12-2d28-e063-6394a90ae42a2025-11-20WarningsExact identifier
ndc (package): 52410-8054-5
ndc (product): 52410-8054
ndc11 (package): 52410805405
spl id: 440b711a-de13-2d28-e063-6394a90ae42a
spl set id: 440b711a-de12-2d28-e063-6394a90ae42a

Reported adverse events (FAERS/openFDA)#

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