Label: DAVV 2%MINOXIDIL TOPICAL SOLUTION WOMENS HAIR REGROWTH TREATMENT- hair loss product liquid
- NDC Code(s): 82372-011-01
- Packager: Good Manager Holdings Inc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated October 25, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- ASK DOCTOR
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DO NOT USE
Do not use if
• Your hair loss occurs at the front of the scalp.
• Minoxidit topical solution 2% is not intended for treating frontal baldness or a receding hairline.
• There is a family history of hair loss.
• Your hair loss is sudden or appears in patches.
• The cause of your hair loss is unknown.
• You are under 18 years of age. Do not use it on infants or children.
• Your scalp is red, inflamed, infected, irritated, or painful.
• Other medications are applied to the scalp. - KEEP OUT OF REACH OF CHILDREN
- PURPOSE
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WHEN USING
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. Results may occur at 2 months with twice a day usage. For some people, you may need to use this product for at least 4 months before you see results.
• the amount of hair regrowth is different for each people. This product will not work for all people. - STOP USE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
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INACTIVE INGREDIENT
WATER, GLYCERIN, BUTYLENE GLYCOL, PANTHENOL, TRIPEPTIDE-1, AZELAIC ACID, NIACINAMIDE, MENTHA ARVENSIS LEAF EXTRACT, HYDRANGEA MACROPHYLLA LEAF EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, PORTULACA OLERACEA EXTRACT, CHRYSANTHELLUM INDICUM EXTRACT, SOPHORA ANGUSTIFOLIA ROOT A EXTRACT, CENTELLA ASIATICA ROOT EXTRACT, CURCUMIN, HYDROLYZED WHEAT PROTEIN, MOROCCAN NUT OIL, ROSA CANINA FRUIT OIL, SODIUM HYALURONATE, BIOTIN, RETINOL, HYDROXYACETOPHENONE, 1,2-HEXANEDIOL, DISODIUM EDTA.
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DAVV 2%MINOXIDIL TOPICAL SOLUTION WOMENS HAIR REGROWTH TREATMENT
hair loss product liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82372-011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 2 mg in 100 mL Inactive Ingredients Ingredient Name Strength PANTHENOL (UNII: WV9CM0O67Z) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Product Characteristics Color brown Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82372-011-01 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/10/2024 Labeler - Good Manager Holdings Inc (118382673) Establishment Name Address ID/FEI Business Operations Good Manager Holdings Inc 118382673 manufacture(82372-011)