Label: VIOFAIRY 5% MINOXIDIL SPRAY.- 5% minoxidil spray. liquid
- NDC Code(s): 83804-105-01
- Packager: Shenzhen Shandian Jingling Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 31, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
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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
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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 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. - Ask Doctor
- Keep Oot Of Reach Of Children
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Directions
.Apply 1ml(5 Sprays) twice a day. Once in the morning and another time in the evening before bed
.Spray directly on top of the scalp in the area to be treated Using more than directed or more often will not improve results
. Continued use is necessary to increase and then maintain your hair regrowth .
. Discontinuing use may result in hair loss. - Other information
- Inactive ingredients
- Questions
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
VIOFAIRY 5% MINOXIDIL SPRAY.
5% minoxidil spray. liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83804-105 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 5 g in 100 mL Inactive Ingredients Ingredient Name Strength .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I) ALCOHOL (UNII: 3K9958V90M) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) BIOTIN (UNII: 6SO6U10H04) WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83804-105-01 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/30/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 01/30/2024 Labeler - Shenzhen Shandian Jingling Technology Co., Ltd. (418636058) Establishment Name Address ID/FEI Business Operations Shenzhen Shandian Jingling Technology Co., Ltd. 418636058 manufacture(83804-105)