Label: RAPHE PHARMACEUTIQUE- minoxidil liquid
- NDC Code(s): 82627-006-01, 82627-006-02
- Packager: AmWiner & Raphe Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated September 2, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
PRINCIPAL DISPLAY PANEL
EXTRA STRENGTH MINOXIDIL SOLUTION FOR MEN & WOMEN
Active Ingredient: Minoxidil Sulfate 5% w/v
Purpose: Anti-Hair Loss
Uses: Helps Reactivate Hair Follicles, and Increase Hair Volume and Density
Helps Eliminate Recurrence of Hair Loss.
Warnings:
For external use only
Ask a doctor before use if condition covers a large area.
When using this product avoid contact with the eyes. If contact occurs, rinse your eyes thoroughly with water.
Stop use and ask a doctor if condition worsens or does not improve after regular use of the product as directed.
Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center right away.
Directions
Apply to affected area one ml two times daily or as directed by the physician!
Ingredients: Alcohol, Water, Propylene Glycol, Minoxidil, Acetyl Tyrosine, Panthenol, Green Tea Extract, Keratin Amino Acid, Isoflavone, Biotin, Ketoconazole, Coco amido-Propyl Betaine, Menthol, Zinc Pyrithione.
Other information: Store at 59° to 77°F (15° to 25°C)
For Questions Call 1-469-428-5508
-
INGREDIENTS AND APPEARANCE
RAPHE PHARMACEUTIQUE
minoxidil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82627-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 50 mg in 50 mg Product Characteristics Color yellow (Light sparkle yellowish solution) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82627-006-02 1 in 1 BOX 09/02/2023 1 NDC:82627-006-01 50 mg in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 09/02/2023 Labeler - AmWiner & Raphe Holdings LLC (113433590) Establishment Name Address ID/FEI Business Operations AmWiner & Raphe Holdings LLC 113433590 manufacture(82627-006)