FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
RIMPORTS INC.
Effective date
2018-03-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:54:54

Label at a glance#

ProductHand Sanitizer
Active ingredientBENZETHONIUM CHLORIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:
Benzethonium Chloride 0.105%

OTC - PURPOSE SECTION

Purpose

Antiseptic

OTC - STOP USE SECTION

Stop use and ask a doctor if redness appears and persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. If swallowed, contact medical help or poison control.

DOSAGE & ADMINISTRATION SECTION

Directions Spray on palm and rub your hands together until absorbed.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, PEG-40 Hydrogenated Castor Oil, Betaine, Fragrance, Eucalyptus Globulus Leaf Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Phenoxyethanol, Diazolidinyl Urea, Palmitamidopropyltrimonium Chloride, Sodium Citrate, Disodium EDTA.

OTHER SAFETY INFORMATION

Other Information

May damage fabrics and surfaces.

INDICATIONS & USAGE SECTION

Uses

For waterless hand washing to decrease bacteria on skin. Recommended for repeated use.

WARNINGS SECTION

WARNINGS:

For external use only.

OTC - WHEN USING SECTION

When using this product, Avoid face, eyes or sensitive areas. If contact occurs flush thoroughly with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle labelimage of bottle label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72131-001-012020-01-31C16284748780-19d75b9d1-18f6-f424-e053-dadaa90a57ce66b9f9cd-be22-181e-e053-2991aa0a1f22

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72131-001-01Hand Sanitizer59 mL in 1 BOTTLE, PLASTICGEL592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72131-001HAND SANITIZER (BENZETHONIUM CHLORIDE) GEL [RIMPORTS INC.]2Legacy NDC, 1 package rows20180315_66b9f9cd-be22-181e-e053-2991aa0a1f22.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72131-00172131-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
BETAINE3SCV180C9WIACT
EUCALYPTUS GLOBULUS LEAFS546YLW6E6IACT
ROSEMARY OIL8LGU7VM393IACT
BENZETHONIUM CHLORIDEPH41D05744ACTIB
WATER059QF0KO0RIACT
PALMITAMIDOPROPYLTRIMONIUM CHLORIDEN2U96D202FIACT
SODIUM CITRATE1Q73Q2JULRIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT

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
676dbe7b-e54f-2b2f-e053-2a91aa0ab40766b9f9cd-be22-181e-e053-2991aa0a1f222018-03-15WarningsExact identifier
spl id: 676dbe7b-e54f-2b2f-e053-2a91aa0ab407
spl set id: 66b9f9cd-be22-181e-e053-2991aa0a1f22

Reported adverse events (FAERS/openFDA)#

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