AmeriDerm Foam Alcohol Hand Sanitizer

Manufacturer
Shield Line LLC
Effective date
2016-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:46:53

Label at a glance#

ProductAmeriDerm Foam Alcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

for sanitizing to reduce bacteria on skin

Dosage and administration

apply one shot of foaming sanitizer to dry hands rub into skin no rinsing required

Label contents#

Full prescribing information#

DRUG FACTS

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • for sanitizing to reduce bacteria on skin

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY

Flammable: Keep away from fire or flame

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes. In case of eye contact, flush eyes with water

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

  • apply one shot of foaming sanitizer to dry hands
  • rub into skin
  • no rinsing required

INACTIVE INGREDIENT SECTION

BIS-PEG-12 Dimethicone, Isopropyl Alcohol, PEG-12 Dimethicone Crosspolymer, Propylene Glycol, Water

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANELPRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN1
616805ethanol 0.7 ML/ML Topical FoamSCD1
616805ethanol 70 % Topical FoamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52410-8080-32020-01-31C16284748780-19d75b9d0-162d-f424-e053-dadaa90a57ce34ca8ec4-782a-053e-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52410-8080-3AmeriDerm Foam Alcohol Hand Sanitizer1000 mL in 1 BOTTLELIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52410-8080AMERIDERM FOAM ALCOHOL HAND SANITIZER (ETHYL ALCOHOL) LIQUID [SHIELD LINE LLC]1Legacy NDC, 1 package rows20160824_34ca8ec4-782a-053e-e054-00144ff88e88.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
52410-808052410-8080-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
34ca8ec4-782b-053e-e054-00144ff88e8834ca8ec4-782a-053e-e054-00144ff88e882016-06-08WarningsExact identifier
spl id: 34ca8ec4-782b-053e-e054-00144ff88e88
spl set id: 34ca8ec4-782a-053e-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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