FDA.reportPublic FDA data

Green Guard Antiseptic Spray

Manufacturer
Unifirst First Aid Corporation | Safetec of America, Inc.
Effective date
2025-09-08
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:12:59

Label at a glance#

ProductAntiseptic
Active ingredientBENZALKONIUM CHLORIDE
Label structure14 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Purpose

First aid antiseptic

INDICATIONS & USAGE SECTION

Uses

First aid to help prevent infection in minor cuts, scrapes and burns.

WARNINGS SECTION

Warnings

For external use only.

OTC - DO NOT USE SECTION

Do not use

  • in the eyes or apply over large areas of the body
  • longer than one week unless directed by a doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • deep or puncture wounds, animal bites, or serious burns

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition persists or gets worse

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.

DOSAGE & ADMINISTRATION SECTION

Directions

  • clean affected area
  • spray a small amount of this product on the area1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first

OTHER SAFETY INFORMATION

Other information

  • shake well
  • store at room temperature

INACTIVE INGREDIENT SECTION

Inactive ingredients

alcohol, water

OTC - QUESTIONS SECTION

Questions or comments? 1-800-869-6970

Green Guard Antiseptic Spray Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antiseptic spray

Benzalkonium Chloride 0.13%

First Aid Antiseptic

Treats minor cuts, scrapes and abrasions

Helps prevent infection

Store at room temperature

GREEN GUARD ®

2 fl oz (59.1 mL)

30013001

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039012benzalkonium chloride 0.13 % Topical SprayPSN9
1039012benzalkonium chloride 1.3 MG/ML Topical SpraySCD9
1039012benzalkonium chloride 0.13 % Topical SpraySY9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47682-316-02Antiseptic0.0591 L in 1 BOTTLE, SPRAYLIQUID0.05919

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47682-31647682-316-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
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
AntisepticBENZALKONIUM CHLORIDEUnifirst First Aid Corporationa0f58025-2c50-45dc-94db-cacbd4cf604c2025-09-08WarningsExact identifier
ndc (package): 47682-316-02
ndc (product): 47682-316
ndc11 (package): 47682031602
spl id: 3e4ed1ac-fdd3-6cfb-e063-6294a90a58c0
spl set id: a0f58025-2c50-45dc-94db-cacbd4cf604c

Reported adverse events (FAERS/openFDA)#

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