GREEN GUARD® Antiseptic spray

Manufacturer
Ultra Distributors Inc
Effective date
2020-12-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:35:39

Label at a glance#

ProductGREEN GUARD First Aid Antiseptic
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

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

Dosage and administration

clean affected area & spray 1 to 3 times daily may be covered with a sterile bandage not to be used on children under 12 years of age

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

  • near eyes or mucous membranes
  • on deep or puncture wounds, animal bites, or serious burns
  • over large areas of the body
  • more than one week unless directed by a doctor

Stop use and ask a doctor

OTC - STOP USE SECTION

if condition persists or gets worse

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean affected area & spray 1 to 3 times daily
  • may be covered with a sterile bandage
  • not to be used on children under 12 years of age

Inactive ingredients

INACTIVE INGREDIENT SECTION

ethyl alcohol, purified water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-869-6970

SPL UNCLASSIFIED SECTION

Treats minor cuts, scrapes and abrasions

Helps prevent infection

Store at 68°-77°F (20°-25°C)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle labelimage of bottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039012benzalkonium chloride 0.13 % Topical SprayPSN1
1039012benzalkonium chloride 1.3 MG/ML Topical SpraySCD1
1039012benzalkonium chloride 0.13 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78495-112-012025-01-30C16284748780-12cef2736-95e5-d83d-e063-dadaa90ab31fGREEN GUARD® Antiseptic spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78495-112-01GREEN GUARD First Aid Antiseptic59.1 mL in 1 BOTTLE, SPRAYSPRAY59.11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78495-112GREEN GUARD FIRST AID ANTISEPTIC (BENZALKONIUM CHLORIDE) SPRAY [ULTRA DISTRIBUTORS INC]1Legacy NDC, 1 package rows20201221_b6e5b0c1-b30b-6d44-e053-2a95a90a33e7.zip

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
78495-11278495-112-01

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
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALCOHOL3K9958V90MIACT

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
b6e5b0c1-b30c-6d44-e053-2a95a90a33e7b6e5b0c1-b30b-6d44-e053-2a95a90a33e72020-12-20WarningsExact identifier
spl id: b6e5b0c1-b30c-6d44-e053-2a95a90a33e7
spl set id: b6e5b0c1-b30b-6d44-e053-2a95a90a33e7

Reported adverse events (FAERS/openFDA)#

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