Gunk Getter Sanitizing

Manufacturer
PeerBasics LLC | Hangzhou Huiji Biotechnology Co.,Ltd
Effective date
2023-08-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:55:57

Label at a glance#

ProductGunk Getter Sanitizing
Active ingredientLAURAMIDOPROPYLAMINE OXIDE, BENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

adults and children 2 years and over: apply to hands. allow skin to dry without wiping. children under 2 years: ask a doctor before use.

Storage and handling

do not store above 105F(41C). may discolor some fabrics. harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride

Lauramide Propyl Dimethyl Oxide Amine

Purpose

OTC - PURPOSE SECTION

Antimicrobial Agent

Surfactant

Antifugal

Use

INDICATIONS & USAGE SECTION

Use to decrase bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

Do not use it you are allergic to any of the ingredients.

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin.
  • do not inhale or ingest.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash develops and continues for more than72 hours.

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

adults and children 2 years and over:

  • apply to hands.
  • allow skin to dry without wiping.
  • children under 2 years: ask a doctor before use.

Other information

STORAGE AND HANDLING SECTION

  • do not store above 105F(41C).
  • may discolor some fabrics.
  • harmful to wood finishes and plastics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water

Glycerol

Fungicide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83590-002-01Gunk Getter Sanitizing80 mL in 1 BOTTLE, SPRAYSPRAY802
83590-002-02Gunk Getter Sanitizing98 mL in 1 BOTTLE, SPRAYSPRAY982
83590-002-03Gunk Getter Sanitizing473 mL in 1 BOTTLE, SPRAYSPRAY4732
83590-002-04Gunk Getter Sanitizing828 mL in 1 BOTTLE, SPRAYSPRAY8282
83590-002-05Gunk Getter Sanitizing946 mL in 1 BOTTLE, SPRAYSPRAY9462

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83590-002GUNK GETTER SANITIZING (BENZALKONIUM CHLORIDE) SPRAY [PEERBASICS LLC]25 package rows20230825_00e75912-7225-114c-e063-6294a90ab9aa.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83590-00283590-002-01, 83590-002-02, 83590-002-03, 83590-002-04, 83590-002-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
03a6805e-6599-ef81-e063-6294a90ad65b00e75912-7225-114c-e063-6294a90ab9aa2023-08-24WarningsExact identifier
spl id: 03a6805e-6599-ef81-e063-6294a90ad65b
spl set id: 00e75912-7225-114c-e063-6294a90ab9aa

Reported adverse events (FAERS/openFDA)#

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