FDA.reportPublic FDA data

GD Disinfectant Wipes

Manufacturer
JRB Group dba/ Grand Destiny Group
Effective date
2020-12-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:59:38

Label at a glance#

ProductGD Disinfectant Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

For sanitizing and to help reduce bacteria on the skin

Dosage and administration

Open the lid and tear off the inner seal. Gently pull out the wipe. Thoroughly wip the skin as desired. Dispose of the used wipe in the trash, do not flush it into the toilet.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride(0.13%)

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses:

INDICATIONS & USAGE SECTION

For sanitizing and to help reduce bacteria on the skin

Warnings:

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

if you are allergic to any of the ingredients.

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. For external use only.

Directions:

DOSAGE & ADMINISTRATION SECTION

Open the lid and tear off the inner seal. Gently pull out the wipe. Thoroughly wip the skin as desired. Dispose of the used wipe in the trash, do not flush it into the toilet.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Sodium benzoate, Propylene glycol, Aloe barbadensis leaf juice, PEG-8 dimethicone, Disodium EDTA, Citric acid.

Package Labeling:50 Wipes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:80 Wipes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81166-00081166-000-50, 81166-000-80

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
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM BENZOATEOJ245FE5EUIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
PEG-8 DIMETHICONEGIA7T764ODIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
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
cf4294a0-c6ab-09ef-e053-2995a90a8eb7b6225859-b7fa-e328-e053-2a95a90a57932021-10-26WarningsExact identifier
spl set id: b6225859-b7fa-e328-e053-2a95a90a5793

Reported adverse events (FAERS/openFDA)#

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