Label: NINCRANE 5% MINOXIDIL FOR MEN- 5% minoxidil for men liquid
- NDC Code(s): 83770-002-01
- Packager: Clearchic, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 10, 2024
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
- Do not use
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Do not use
• You are a woman. • Your level of hair loss is different from that shown on the side of this carton, or your hair loss is on the front of the scalp. Hair Regrowth Treatment is not intended for frontal baldness or receding hairline.
• You have no family history of hair loss.
• Your 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 on babies and children.
• Your scalp is red, inflamed, infected, irritated, or painful.
• You use other medicines on the scalp.
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When Using
1. Do not apply on other parts of the body. For topical use only on the scalp.
2. Avoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cool tap water.
3. Some people have experienced changes in hair color and/or texture.
4. The amount of hair regrowth is different for each person. This product will not work for all men. - Stop Use
- Ask Doctor
- Keep Out Of Reach Of Children
- Directions
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Other information
• See hair loss pictures on side of this carton.
• Before use, read all information on carton and enclosed leaflet.
• Keep this carton, It contains important information.
• Clinical research in mostly white men aged 18-49 years with moderate degrees of hair loss, showed that minoxidil topical solution 5% proves more hair regrowth than minoxidil topical solution 2% for men.
• Store at controlled room temperature between 68°-77°F (2°0-25°C). Keep tightly closed
- Inactive ingredients
- Questions
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NINCRANE 5% MINOXIDIL FOR MEN
5% minoxidil for men liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83770-002 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 ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83770-002-01 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/30/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 10/30/2023 Labeler - Clearchic, Inc. (101430907) Establishment Name Address ID/FEI Business Operations Clearchic, Inc. 101430907 label(83770-002) , manufacture(83770-002)
