5% MINOXIDIL TOPICAL SOLUTION- minoxidil solution 
Gabar Health Sciences Corp.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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5% Minoxidil Topical Solution

​Drug Facts

​Active Ingredient

Minoxidil 5% w/w (without propellant)

​Purpose

Hair regrowth treatment for men

​Use

To regrow hair on the top of the scalp (vertex only, see pictures on side of this carton)

​Warnings

For external use only.

For use by men only.

​Extremely Flammable:​ Avoid fire, flame, or smoking during and immediately following application.

​Do not use if

​Ask a doctor before use if you have heart disease

​When using this product

​Stop use and ask a doctor if

​May be harmful if used when pregnant or breast feeding.

​Keep out of reach of children. ​If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

​Directions

​Other information

​Inactive ingredients

​butylated hydroxytoluene, cetyl alcohol, citric acid anhydrous, dehydrated alcohol, isobutane, lactic acid, n-butane, polysorbate 60, propane, purified water, stearyl alcohol

​Questions?

Manufactured and distributed by:

Gabar Health Sciences Corp., Atlanta, GA 30385

​PRINCIPAL DISPLAY PANEL

​Minoxidil Topical Aerosol, 5% (For Men)

HAIR REGROWTH TREATMENT

​Reactivates hair follicles to stimulate regrowth

Clinically proven to help regrow hair

#1 Dermatologist Recommended Active Ingredient

Easy-to-use-foam unscented

3 MONTH SUPPLY

3 - 60 g (2.11 OZ) CANS

​NOT FOR USE BY WOMEN

Minoxidil Men Carton Label

5% MINOXIDIL TOPICAL SOLUTION 
minoxidil solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82429-200
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
DEHYDRATED ALCOHOL (UNII: 3K9958V90M)  
ISOBUTANE (UNII: BXR49TP611)  
LACTIC ACID (UNII: 33X04XA5AT)  
BUTANE (UNII: 6LV4FOR43R)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
PROPANE (UNII: T75W9911L6)  
WATER (UNII: 059QF0KO0R)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
Product Characteristics
Colorwhite (white to off-white foam) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82429-200-6060 mL in 1 PACKAGE; Type 0: Not a Combination Product10/10/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/10/2022
Labeler - Gabar Health Sciences Corp. (118401847)
Registrant - Gabar Health Sciences Corp. (118401847)
Establishment
NameAddressID/FEIBusiness Operations
Gabar Health Sciences Corp.118401847manufacture(82429-200)

Revised: 11/2022
Document Id: ee253d94-4b61-6e9f-e053-2995a90a4726
Set id: a06766b4-981e-48a7-b4b4-606f9f47f273
Version: 3
Effective Time: 20221122
 
Gabar Health Sciences Corp.