FDA.reportPublic FDA data

Shield

Manufacturer
Benchmark Industrial Inc.
Effective date
2022-10-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:52:14

Label at a glance#

ProductShield
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

adults and children 2 years and over • apply to hands • allow to dry without wiping  children under 2 years • ask a doctor before use

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Use decrease bacteria on skin

Warnings

WARNINGS SECTION

For external use only

Do not use if you are allergic to any of the ingredients

When using this product do not get into eyes. If contact occurs, rinse thoroughly with water

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 2 years and over• apply to hands

• allow to dry without wiping

 children under 2 years• ask a doctor before use

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera, Aqua (Water), Disodium Cocoamphodiacetate, Fragrance, Glycerin, PEG 40 Hydrogenated Castor Oil, Propylene Glycol.

Questions or Comments?

OTC - QUESTIONS SECTION

Call 844-4BENCHMARK

SPL UNCLASSIFIED SECTION

Benchmark Industrial | www.benchmarkproduct.com

Manufactured for:

Benchmark Industrial Inc.              

Columbus, Ohio, USA

Tel: 844 - 4BENCHMARK

www.benchmarkproduct.com

Made in Vietnam

Recyclable packaging

Safe on skin

Store between 40-75°F

Do not flush used wipes

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

PackagingPackaging

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74419-77574419-775-80

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
NameUNIIKind
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
GLYCERINPDC6A3C0OXIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
a6878b29-621a-467c-8672-bf0a05c62b653cb1ba03-9178-4849-8e0f-a8b141a50d0c2022-10-06WarningsExact identifier
spl id: a6878b29-621a-467c-8672-bf0a05c62b65
spl set id: 3cb1ba03-9178-4849-8e0f-a8b141a50d0c

Reported adverse events (FAERS/openFDA)#

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