DS-467 Elevate 2% Minoxidil Liquid

Elevate 2% Minoxidil Liquid by

Drug Labeling and Warnings

Elevate 2% Minoxidil Liquid by is a Otc medication manufactured, distributed, or labeled by Foshan Yilai Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ELEVATE 2% MINOXIDIL LIQUID- elevate 2% minoxidil liquid liquid 
Foshan Yilai Cosmetics Co., Ltd.

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.

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DS-467 Elevate 2% Minoxidil Liquid

MINOXIDIL 2%

Hair regrowth treatment

Do not use if

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

Deionized Water,

Propylen Glycol, Alcohol,

Panax Ginseng, Pro-Vitamin B5.

For external use only.

For use on scalp only.

Avoid contact with eyes.

Keep out of reach of children.

Keep stored at room temperature.

Keep away from fire or flame

Ask a doctor before use if you have heart disease

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. You may need to use this product 2 times a day for at least 4 months before you see results.

The amount of hair regrowth is different for each person. This product will not work for everyone.

Stop use and ask a doctor if

Chest pain, rapid heartbeat, faintness, or dizziness occurs

sudden, unexplained weight gain occurs

Your hands or feet swell

Scalp irritation or redness occurs

Unwanted facial hair growth occurs

You do not see hair regrowth in 4 months

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

May be harmful if used when pregnant or breast-feeding.

ELEVATE 2% MINOXIDIL

is applied to the scalp and used to

stimulate hair growth in adult women.

It’s a spray solution that’s been

approved by the FDA to treat hair loss

and help regrow hair.

Prevent and Stop Hair Loss

Stimulate Hair Growth

Improve Fullness of Hair

Restore Vitality of Hair

Strengthen and Activate Hair Follicles

Store at controlled room temperature 20° to 25°C (68° to 77°F)

Minoxidil may cause side effects.

Discontinue use immediately or tell

your doctor if any of these symptoms

are severe or do not go away: scalp

itching, dryness, scaling, flaking,

irritation, or burning.

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.

Elevate 2% Minoxidil Liquid

ELEVATE 2% MINOXIDIL LIQUID 
elevate 2% minoxidil liquid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 83830-105
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M) 40 mL  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 49 mL  in 100 mL
PANAX GINSENG ROOT WATER (UNII: P9T4K47OM0) 2 mL  in 100 mL
WATER (UNII: 059QF0KO0R) 5 mL  in 100 mL
PANTHENOL (UNII: WV9CM0O67Z) 2 mL  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 83830-105-01100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/27/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/27/202303/07/2024
Labeler - Foshan Yilai Cosmetics Co., Ltd. (602056456)
Registrant - Foshan Yilai Cosmetics Co., Ltd. (602056456)
Establishment
NameAddressID/FEIBusiness Operations
Foshan Yilai Cosmetics Co., Ltd.602056456manufacture(83830-105)

Revised: 3/2024