Label: IBEALEE 5% MINOXIDIL HAIR GROWTH SOLUTION liquid
- NDC Code(s): 83809-012-01, 83809-012-02
- Packager: Shenzhen Yikai Electronic Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
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Do not use
-You have no family history of hair loss,hair loss is sudden and/or patchy.
-You do not know the reason for your hair loss.
-You are under 18 years of age.Do not use it on bables and children your scalp is red.inflamed,infected, imitated,or painful.
-You use other medicines on the scalp
-Ask a Doctor before use of you have Heart disease. -
When Using
-Do not apply to 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 imitation or redness occurs
-May be harmful if used when pregnant or breast-feeding
-Keep Out Of Reach Of Chlidren: if swallowed,get medical help or contact a Poison Control Center right away. - Keep Oot Of Reach Of Children
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Directions
-Apply 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 lncrease and then malntain your hair regrowth
-Discontinuing use may result in hair loss - Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
IBEALEE 5% MINOXIDIL HAIR GROWTH SOLUTION
ibealee 5% minoxidil hair growth solution liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83809-012 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 WATER (UNII: 059QF0KO0R) ROSE OIL (UNII: WUB68Y35M7) .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I) LAVENDER OIL (UNII: ZBP1YXW0H8) CASTOR OIL (UNII: D5340Y2I9G) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CYMBOPOGON CITRATUS LEAF (UNII: 06JMS448M5) CHAMOMILE (UNII: FGL3685T2X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83809-012-01 20 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/04/2023 2 NDC:83809-012-02 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/04/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 12/04/2023 Labeler - Shenzhen Yikai Electronic Technology Co., Ltd. (700426808) Establishment Name Address ID/FEI Business Operations Shenzhen Yikai Electronic Technology Co., Ltd. 700426808 manufacture(83809-012) , label(83809-012)
