FDA.reportPublic FDA data

GHOSTMedica Hand Sanitizer

Manufacturer
Biomedical Research and Development Inc
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:17:33

Label at a glance#

ProductGHOSTMedica Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
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.

Storage and handling

store between 15-30C (59-86F) avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

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

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

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. 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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, propylene glycol

Questions or Comments?

OTC - QUESTIONS SECTION

emergency contact number 1-800-778-4247

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 mL NDC: 80713-001-02

50mL50mL

236 mL NDC: 00000-001-08

236mL236mL

1000 mL NDC: 80713-001-10

1000 mL1000 mL

3785 mL NDC: 80713-001-37

3785 mL3785 mL3785 mL back3785 mL back

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80713-00180713-001-02, 80713-001-08, 80713-001-10, 80713-001-37

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
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

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
ee9c4d1d-f616-74ad-e053-2a95a90ad6d3adc0024e-aaf0-eafb-e053-2a95a90a99692022-11-29WarningsExact identifier
spl set id: adc0024e-aaf0-eafb-e053-2a95a90a9969

Reported adverse events (FAERS/openFDA)#

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