FDA.reportPublic FDA data

GSD Anti-Bacterial Gel

Manufacturer
Good Spirits Distilling, LLC
Effective date
2020-06-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:25:00

Label at a glance#

ProductGSD Anti Bacterial
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient[s]

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 73.30% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use[s]

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

  • on children less than 2 months of age
  • on open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash occurs. These may be signs of a serious condition.

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

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

SPL UNCLASSIFIED SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

  • Hydroxypropylcellulose, Aqua (water), Lauryl Lactate and MyristylLactate and cetylLactate, Glycerin, Lemongrass Essential Oil

Package Labeling: 1750ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling: 1000ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling: 750ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Package Labeling: 500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

Package Labeling: 375ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5Label5

Package Labeling: 250ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label6Label6

Package Labeling: 100ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label7Label7

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78631-00078631-000-06, 78631-000-05, 78631-000-04, 78631-000-03, 78631-000-02, 78631-000-01, 78631-000-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYDROXYPROPYL CELLULOSE, UNSPECIFIED9XZ8H6N6OHIACT
WATER059QF0KO0RIACT
LAURYL LACTATEG5SU0BFK7OIACT
MYRISTYL LACTATE1D822OC34XIACT
CETYL LACTATEA7EVH2RK4OIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB

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
e963ee29-7a99-3dfe-e053-2a95a90a676ca85db494-34a0-5e86-e053-2a95a90a79672022-09-23WarningsExact identifier
spl set id: a85db494-34a0-5e86-e053-2a95a90a7967

Reported adverse events (FAERS/openFDA)#

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