GSD Good Hygiene Defense Wet Wipes

Manufacturer
JoCo Sales & Marketing, Inc.
Effective date
2020-08-31
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:16:35

Label at a glance#

ProductGSD Good Hygiene Defense Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

For hand washing to decrease bacteria on the skin. Recommended for repeat use.

Dosage and administration

Open resealable label and pull one sheet from pack. Thoroughly clean hands or affected area and discard in receptacle, and do not flush. Allow to dry without wiping. Be sure to reseal label complete to retain moisture.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.10%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand washing to decrease bacteria on the skin. Recommended for repeat use.

Warnings

WARNINGS SECTION

  • For external use only.
  • Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.

Do not use 

OTC - DO NOT USE SECTION

  • if you are allergic to any of the ingredients.
  • Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.

Keep out of reach of children 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • unless under adult supervision.
  • If swallowed, get medical help, or contact a Poison Control Center immediately.

Directions of use

DOSAGE & ADMINISTRATION SECTION

  • Open resealable label and pull one sheet from pack. Thoroughly clean hands or affected area and discard in receptacle, and do not flush. Allow to dry without wiping. Be sure to reseal label complete to retain moisture.

Other Information

SPL UNCLASSIFIED SECTION

  • Store at room temperature.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

  • Water (Aqua), Glycerol, Propanediol, Aloe Vera Extract, Amino acid moisturizer, Hexadecylpyridinium Chloride, Chlorphenesin, Vitamin E, Citric acid, Sodium citrate.

Package Labeling:20ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20ct Wipes20ct Wipes

Package Labeling:80ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80ct Wipes80ct Wipes

Package Labeling: 77784-001-21, 200ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

200ct Label200ct Label200ct Drug Facts Panel200ct Drug Facts Panel

77784-001-32 package label 80 wipes in a bag, 4 bags in a box. 320 Wipes total.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

320ct Label320ct Label320ct Drug Facts320ct Drug Facts

800ct Package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Updated 800ct Label FrontUpdated 800ct Label Front800ct Drug Facts Panel800ct Drug Facts Panel

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77784-00177784-001-20, 77784-001-80, 77784-001-21, 77784-001-32, 77784-001-81

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
eb74f3f3-21d7-2200-e053-2995a90a1e184df1c19e-07d7-4afd-acfd-5a9c031e599e2022-10-20WarningsExact identifier
spl set id: 4df1c19e-07d7-4afd-acfd-5a9c031e599e

Reported adverse events (FAERS/openFDA)#

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