FDA.reportPublic FDA data

SCENTFULL FOAMING HAND SANITIZER

Manufacturer
SCENT THEORY PRODUCTS LLC
Effective date
2022-01-16
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:16:19

Label at a glance#

ProductSCENTFULL FOAMING HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

decreases bacteria on hands

Dosage and administration

Dispense a palm-sized amount onto hands. Rub hands together until dry.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.1%

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USES

INDICATIONS & USAGE SECTION

  • decreases bacteria on hands

WARNINGS

WARNINGS SECTION

Use only as directed. For external use only.

When using this product. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation and redness develop or increase.

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

Dispense a palm-sized amount onto hands.

  • Rub hands together until dry.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

COCONUT VANILLA:  Water (Aqua), PEG-40 Hydrogenated Castor Oil, Glycerin, Fragrance (Parfum), Didecyldimonium Chloride, Phenoxyethanol, Polyaminopropyl Biguanide, Citric Acid, Vanilla Planifolia Fruit Oil, Yellow 5 (CI 19140), Red 33 (CI 17200), Blue 1 (CI 42090).

EUCALYPTUS SPEARMINT: Water (Aqua), PEG-40 Hydrogenated Castor Oil, Glycerin, Fragrance (Parfum), Didecyldimonium Chloride, Phenoxyethanol, Polyaminopropyl Biguanide, Citric Acid, Eucalyptus Globulus Leaf Oil, Blue 1 (CI 42090), Yellow 5 (CI 19140).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Foaming Hand Sanitizer_Coconut-Vanilla_50mL01b LBL_Foaming Hand Sanitizer_Coconut-Vanilla_50mL

01b LBL_Foaming Hand Sanitizer_Eucalyptus-Spearmint_50mL01b LBL_Foaming Hand Sanitizer_Eucalyptus-Spearmint_50mL

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76891-11976891-119-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
GLYCERINPDC6A3C0OXIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYAMINOPROPYL BIGUANIDEDT9D8Z79ETIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
VANILLA PLANIFOLIA OIL0A3F415158IACT
EUCALYPTUS OIL2R04ONI662IACT
D&C RED NO. 339DBA0SBB0LIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
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
d5b80c45-8351-7a42-e053-2995a90a7484b401d0ad-c8ed-4369-8e03-2ad84af5dffd2022-01-16WarningsExact identifier
spl id: d5b80c45-8351-7a42-e053-2995a90a7484
spl set id: b401d0ad-c8ed-4369-8e03-2ad84af5dffd

Reported adverse events (FAERS/openFDA)#

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