FDA.reportPublic FDA data

GENTLE HAND SANITIZER

Manufacturer
Nature's Organics, LLC | Health Specialty
Effective date
2020-03-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:38:39

Label at a glance#

ProductGENTLE HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand sanitizing to reduce bacteria on the skin. Recommended for repeated use.

Dosage and administration

Spray the hands and rub together briskly to cover all surfaces.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.1%

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

USES

INDICATIONS & USAGE SECTION

For hand sanitizing to reduce bacteria on the skin. Recommended for repeated use.

WARNINGS

WARNINGS SECTION

For external use only.

Avoid direct contact with eyes. In case of eye contact, please flush the eyes with water.

Contact a doctor if irritation or redness persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help and/or contact a poison control center immediately.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Spray the hands and rub together briskly to cover all surfaces.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Benzoic Acid, Ethylhexyl-glycerin, Glycereth-2 Cocoate, Dihydroxypropyl PEG-5, Linoleammonium Chloride, Behetrimonium Chloride, Potassium Hydroxide, Dihydroxyethyl Cocamine Oxide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Hand Sanitizer Spray_4 oz01b LBL_Hand Sanitizer Spray_4 oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73725-110-112024-03-27C16284748780-1d6a99b39-bc8d-a426-e053-dadaa90af4c2NATURE'S BABY - GENTLE HAND SANITIZER
73725-110-112022-01-28C16284748780-1d6a99b39-bc8d-a426-e053-dadaa90af4c2NATURE'S BABY - GENTLE HAND SANITIZER

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73725-11073725-110-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
BENZOIC ACID8SKN0B0MIMIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERETH-2 COCOATEJWM00VS7HCIACT
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE0Y0NQR2GH1IACT
BEHENTRIMONIUM CHLORIDEX7GNG3S47TIACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT

Source Document#

Source XML · Source PDF

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
14abd794-128d-43c0-e063-6294a90a9af532269306-3386-4d3f-9d0b-34dd9e8ca93d2024-03-27WarningsExact identifier
spl set id: 32269306-3386-4d3f-9d0b-34dd9e8ca93d

Reported adverse events (FAERS/openFDA)#

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