Label: ELEVATE 2% MINOXIDIL HAIR LIQUID liquid
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- NDC Code(s): 78098-304-01
- Packager: GUANGZHOU NODA PHARMACEUTICAL TECHNOLOGY INCORPORATED CO., LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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 11, 2023
If you are a consumer or patient please visit this version.
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- ACTIVE INGREDIENT
- PURPOSE
- DO NOT USE
- WARNINGS
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INACTIVE INGREDIENT
Aqua, Propylene Glycol, Glycerin, Panthenol, Zingiber Officinale (Ginger) Extract,Camellia Sinensis Leaf Extract, Cocos Nucifera (Coconut) Oil, Biotin, Myristica Fragrans (Nutmeg) Extract, Boswellia Serrata Gum, Polygonum Multiflorum Extract, Sarcosine, Hydroxyacetophenone, 1,2-Hexanediol, Fragrance.
- STORAGE AND HANDLING
- DESCRIPTION
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Spray 1ml (5 sprays) twice a day. Once in the morning and another time in the evening before bed. Use only on fully dry hair. Spray directly on top of the scalp of hair loss area. Results can vary and take time but we recommend at least 3-5 months of usage.
*Using more than directed or more often will not improve results. Continued use is necessary to increase and keep your hair regrowth, or hair loss can begin again*
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ELEVATE 2% MINOXIDIL HAIR LIQUID
elevate 2% minoxidil hair liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78098-304 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 2 g in 100 mL Inactive Ingredients Ingredient Name Strength COCONUT OIL (UNII: Q9L0O73W7L) 1 mL in 100 mL SARCOSINE (UNII: Z711V88R5F) 0.5 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 5 mL in 100 mL WATER (UNII: 059QF0KO0R) 40.95 mL in 100 mL PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 38 mL in 100 mL INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) 0.5 mL in 100 mL GINGER OIL (UNII: SAS9Z1SVUK) 3 mL in 100 mL PANTOTHENIC ACID (UNII: 19F5HK2737) 5 mL in 100 mL GREEN TEA LEAF (UNII: W2ZU1RY8B0) 1 mL in 100 mL HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) 0.5 mL in 100 mL BIOTIN (UNII: 6SO6U10H04) 1 mL in 100 mL NUTMEG (UNII: AEE24M3MQ9) 0.5 mL in 100 mL REYNOUTRIA MULTIFLORA ROOT (UNII: AUZ3VD75MC) 0.5 mL in 100 mL 1,2-HEXANEDIOL (UNII: TR046Y3K1G) 0.5 mL in 100 mL FRAGRANCE MINT ORC2000774 (UNII: G7LK3FFB99) 0.05 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78098-304-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 05/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/01/2022 Labeler - GUANGZHOU NODA PHARMACEUTICAL TECHNOLOGY INCORPORATED CO., LTD (554457375) Registrant - GUANGZHOU NODA PHARMACEUTICAL TECHNOLOGY INCORPORATED CO., LTD (554457375) Establishment Name Address ID/FEI Business Operations GUANGZHOU NODA PHARMACEUTICAL TECHNOLOGY INCORPORATED CO., LTD 554457375 manufacture(78098-304)
