FDA.reportPublic FDA data

Star-San Foaming Hand Sanitizer

Manufacturer
Diamond Chemical Co Inc
Effective date
2022-11-17
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 21:47:32

Label at a glance#

ProductStar-San Foaming Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl Alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • For handwashing to decrease bacteria on the skin after changing diapers, assisting ill persons or before contact with a person under medical care or treatment.
  • Recommended for repeated use.

WARNINGS SECTION

Warnings

  • For external use only

OTC - WHEN USING SECTION

  • Keep out of eyes, ears or mouth.

OTC - STOP USE SECTION

  • Discontinue us if irritation occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

OTHER SAFETY INFORMATION

FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.

DOSAGE & ADMINISTRATION SECTION

Directions

  • If hands are visibly soiled, wash with soap and water and dry hands.
  • Wet hands thoroughly with product, especially the areas under the fingernails and allow to dry without rinsing.

INACTIVE INGREDIENT SECTION

Inactive ingredients benzalkonium chloride, chlorhexidine gluconate, isopropyl alcohol, PEG-10 dimethicone, PEG-14M, phenoxyethanol, polyquaternium 10, water

OTC - QUESTIONS SECTION

Questions?

Call 201-935-4300 for information.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

STAR-SAN™

Waterless Foaming Hand Sanitizer

Meets and exceeds CDC requirements

Kills 99.9% of most germs in 15 seconds

1000 ML CARTRIDGE

MADE IN THE USA

STARCO CHEMICAL

A Division of Diamond Chemical Co. Inc.

LABEL SERIES E - StarSanLABEL SERIES E - StarSan

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
72177-18572177-185-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOXYETHANOLHIE492ZZ3TIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
CHLORHEXIDINE GLUCONATEMOR84MUD8EIACT
ISOPROPYL ALCOHOLND2M416302IACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)GMR4PEN8PKIACT
PEG-10 DIMETHICONE (600 CST)8PR7V1SVM0IACT
PEG-14 1-((METHYLPHENYL)ETHYL)PHENYL ETHER AMMONIUM SULFATES4S9783N13IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
5b69c076-20c0-4180-83d1-5da977174a1dba6f426d-43b1-4686-e053-2a95a90a87942022-11-17WarningsExact identifier
spl id: 5b69c076-20c0-4180-83d1-5da977174a1d
spl set id: ba6f426d-43b1-4686-e053-2a95a90a8794

Reported adverse events (FAERS/openFDA)#

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