Label: BIOTIN- hair liquid
- NDC Code(s): 83872-285-01
- Packager: Shenzhen Xiaomai Manufacturing Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated July 9, 2024
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- 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. - Ask Doctor
- Keep Oot Of Reach Of Children
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BIOTIN
hair liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83872-285 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) BIOTIN 2 g in 30 mL Inactive Ingredients Ingredient Name Strength COCOS NUCIFERA WHOLE (UNII: 245J88W96L) RICINUS COMMUNIS WHOLE (UNII: Q94QWM85RF) OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES (UNII: XO45V955LT) ARGANIA SPINOSA LEAF (UNII: 51XV5WTF7E) TOCOPHEROL (UNII: R0ZB2556P8) SIMMONDSIA CHINENSIS LEAF (UNII: 67G221EK95) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83872-285-01 30 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product 07/10/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 07/10/2024 Labeler - Shenzhen Xiaomai Manufacturing Co., Ltd. (712999147) Establishment Name Address ID/FEI Business Operations Shenzhen Xiaomai Manufacturing Co., Ltd. 712999147 manufacture(83872-285)