SafeShield Hand Sanitizer

Manufacturer
The Trend Innovations Company Inc.
Effective date
2022-10-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:51:22

Label at a glance#

ProductSafeShield Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

• to decrease bacteria on the skin that could cause disease • recommended for repeated use.

Dosage and administration

• wet hands thoroughly with product and allow to dry without wiping • for children under 6, use only under adult supervision • not recommended for infants.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70 %

Purpose

OTC - PURPOSE SECTION

antiseptic

Uses

INDICATIONS & USAGE SECTION

• to decrease bacteria on the skin that could cause disease • recommended for repeated use.

Warnings

WARNINGS SECTION

Flammable. keep away from fire or flame.

For external use only.

When using this product 

OTC - WHEN USING SECTION

keep out of eyes. In case of contact with eyes, flushthoroughly with water • avoid contact with broken skin / do not inhale or ingest.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash or irritation develops and lasts for more than 72 hours.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • • wet hands thoroughly with product and allow to dry without wiping • for children under 6, use only under adult supervision • not recommended for infants.

Other information

SPL UNCLASSIFIED SECTION

  • • do not store above 105°F • may discolor some fabrics • harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua, Glycerin, Carbomer, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

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
79135-00979135-009-05

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
eb5080ed-2f21-b5a8-e053-2995a90ae49da8b10d99-5aa4-0a78-e053-2995a90a47362022-10-18WarningsExact identifier
spl id: eb5080ed-2f21-b5a8-e053-2995a90ae49d
spl set id: a8b10d99-5aa4-0a78-e053-2995a90a4736

Reported adverse events (FAERS/openFDA)#

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