Rory For Women Minoxidil Topical Solution

Rory for Women by

Drug Labeling and Warnings

Rory for Women by is a Otc medication manufactured, distributed, or labeled by Roman Health Ventures Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

RORY FOR WOMEN HAIR REGROWTH TREATMENT- minoxidil solution 
Roman Health Ventures Inc.

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Rory For Women Minoxidil Topical Solution

Drug Facts

Active ingredient

Minoxidil 2% w/v

Purpose

Hair regrowth treatment

Use to regrow hair on the scalp

Warnings

For external use only.
Flammable: Keep away from fire or flame

Do not use if

  • your degree of hair loss is different than that shown on the side of this carton, because this product may not work for you.
  • you have no family history of hair loss
  • your hair loss is sudden and/or patchy
  • your hair loss is associated with childbirth
  • you do not know the reason for your hair loss
  • you are under 18 years of age. Do not use on babies and children.
  • your scalp is red, inflamed, infected, irritated, or painful
  • you use other medicines on the scalp

Ask a doctor before use if you have heart disease

When using this product

  • do not apply on other parts of the body
  • avoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cool tap water.
  • some people have experienced changes in hair color and/or texture
  • it takes time to regrow hair. You may need to use this product 2 times for at least 4 months before you see results.
  • the amount of hair regrowth is different for each person. This product will not work for everyone.

Stop use and ask a doctor if

  • chest pain, rapid heartbeat, faintness, or dizziness occurs
  • sudden, unexplained weight gain occurs
  • your hands or feet swell
  • scalp irritation or redness occurs
  • unwanted facial hair growth occurs
  • you do not see hair regrowth in 4 months

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.

Directions

  • apply one ml with dropper 2 times a day directly onto the scalp in the hair loss area
  • using more or more often will not improve results
  • continued use is necessary to increase and keep your hair regrowth, or hair loss will begin again

Other information

  • see hair loss pictures on side of this carton
  • before use, read all information on carton and enclosed leaflet
  • keep the carton. It contains important information.
  • In clinical studies of mostly white women aged 18 to 45 years with mild to moderate degrees of hair loss, the following response to 2% minoxidil topical solution was reported: 19% of women reported moderate hair regrowth after using 2% minoxidil topical solution for 8 months (19% had moderate regrowth, 40% had minimal regrowth). This compares with 7% of women reportig moderate hair regrowth after using the placebo, the liquid without minoxidil in it, for 8 months (7% had moderate regrowth; 33% had minimal regrowth).
  • store at USP controlled room temperature 20° to 25°C (68° to 77°F)

Inactive ingredients alcohol, propylene glycol, purified water

Questions? 1-424-347-6299 between 9:30 am and 9:00 pm ET, Monday–Friday.

*This product is not affiliated with, manufactured by, or produced by teh makers or owners of Rogaine®.

Distributed by: Roman Health Ventures, New York, NY 10003

Compare to the active ingredient in Women's Rogaine®*

NDC: 72484-085-03
RORY For Women
Minoxidil Topical Solution, USP 2%
HAIR REGROWTH TREATMENT

Reactivates Hair Follicles to Stimulate Regrowth
Clinically Proven to Help Regrow Hair
For best results: Apply directly to scalp twice daily.
Unscented
One month supply
One 60 mL (2 fl oz) Bottle

RORY_Minoxidil Final

RORY FOR WOMEN  HAIR REGROWTH TREATMENT
minoxidil solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 72484-085
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 72484-085-031 in 1 CARTON06/10/202012/06/2021
160 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07817606/10/202012/06/2021
Labeler - Roman Health Ventures Inc. (081317350)

Revised: 12/2021