5% MINOXIDIL FOAM- 5% minoxidil foam spray, suspension 
Consilii LLC

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83299-022 Completed

Active Ingredient

Minoxidil 5%

Purpose

Hair Regrowth Treatment

Use

to regrow hair on the top of the scalp

Warnings

For external use only

Keep away from fire and flame

Avoid contact with eyes

Do not use

You have no family history of hair loss,hair loss is sudden and/or patchy

you are under 18 years of age.Do not use it on babies and children

When Using

Do not apply on other parts of the body

void contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water

It takes time to regrow hair. You may need to use this product 2 times a day for a least 4 months before you see results, The amount of hair regrowth is different for each person

Stop Use

chest pain, rapid heart beat, faintness, or dizziness occurs

sudden, unexplained weight gain occurs

your hands or feet swell

scalp irritation or redness occurs

Keep Oot Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

Apply half a capful 2 times a day directly to the scalp in the hair loss area

Massage into scalp with fingers, then wash well

Using more than directed or more often will not improve results.

Continued use is necessary to increase and then maintain your hair regrowth

Other information

Before use, read all information on the carton

Store at controlled room temperature 20 to 25 C (68 to 77°F)

Inactive ingredients

Deionized Water,Propylene Glycol,Ethyl Alcohol,Potassium Sorbate,GABA

Questions

Tomumcs@gmail.com

PRINCIPAL DISPLAY PANEL

01

5% MINOXIDIL FOAM 
5% minoxidil foam spray, suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83299-022
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
.GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83299-022-0160 g in 1 BOTTLE; Type 0: Not a Combination Product10/08/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)10/08/202311/21/2024
Labeler - Consilii LLC (118891890)
Establishment
NameAddressID/FEIBusiness Operations
Consilii LLC118891890label(83299-022) , manufacture(83299-022)

Revised: 11/2024
 
Consilii LLC