FDA.reportPublic FDA data

Eco Sanity Hand Sanitizer

Manufacturer
SBC International Group Inc.
Effective date
2021-04-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:47:29

Label at a glance#

ProductEco Sanity Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

Decreases bacteria on the skin.

Dosage and administration

Wet hands thoroughly with product and allow to dry. Children under 6 years of age, use only under adult supervision.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Decreases bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat or flame.

When using this product,

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

redness or irritation develops & persists for more than 72 hours.

Keep out of the 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

  • Wet hands thoroughly with product and allow to dry.
  • Children under 6 years of age, use only under adult supervision.

Other Information

SPL UNCLASSIFIED SECTION

  • Do not store above 105°F (43°C).
  • May discolor some fabrics and surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA, AEC THYME OIL, NATURAL BIOPOLYMERS, LACTIC ACID, ALOE BARBADENSIS LEAF JUICE, GLYCERIN, TRIETHANOLAMINE, POLISORBATE 20, CLOVE OIL, FRAGANCE.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79126-00379126-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
LACTIC ACID, UNSPECIFIED FORM33X04XA5ATIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
POLYSORBATE 207T1F30V5YHIACT
CLOVE OIL578389D6D0IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
bfcc8a7a-1986-0c47-e053-2a95a90a5ff2bccae538-9647-f798-e053-2995a90aab112021-04-12WarningsExact identifier
spl id: bfcc8a7a-1986-0c47-e053-2a95a90a5ff2
spl set id: bccae538-9647-f798-e053-2995a90aab11

Reported adverse events (FAERS/openFDA)#

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