GHOSTMedica Hand Sanitizer by Biomedical Research and Development Inc

GHOSTMedica Hand Sanitizer by

Drug Labeling and Warnings

GHOSTMedica Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Biomedical Research and Development Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GHOSTMEDICA HAND SANITIZER- isopropyl alcohol solution 
Biomedical Research and Development Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredient(s)

Isopropyl Alcohol 70% v/v.

Purpose

Antiseptic

Use

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

Warnings

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

Do not use

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

When using this product 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 irritation or rash occurs.

These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• 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

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

Inactive ingredients

water, propylene glycol

Questions or Comments?

emergency contact number 1-800-778-4247

Package Label - Principal Display Panel

50 mL NDC: 80713-001-02

236 mL NDC: 00000-001-08

1000 mL NDC: 80713-001-10

3785 mL NDC: 80713-001-37

GHOSTMEDICA HAND SANITIZER 
isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80713-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80713-001-02	50 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	08/25/2020
2	NDC: 80713-001-08	236 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	08/25/2020
3	NDC: 80713-001-10	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	08/25/2020
4	NDC: 80713-001-37	3785 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	08/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/25/2020	08/25/2020

Labeler - Biomedical Research and Development Inc (052668394)

Establishment
Name	Address	ID/FEI	Business Operations
Biomedical Research and Development Inc		052668394	manufacture(80713-001)

Revised: 11/2022

Document Id: ee9c4d1d-f616-74ad-e053-2a95a90ad6d3

34390-5

Set id: adc0024e-aaf0-eafb-e053-2a95a90a9969

Version: 4

Effective Time: 20221129