DS-129 Elevate 5% Minoxidil Hair Liquid

Elevate 5% Minoxidil Hair Liquid by

Drug Labeling and Warnings

Elevate 5% Minoxidil Hair 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 5% MINOXIDIL HAIR LIQUID- elevate 5% minoxidil hair 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.

----------

DS-129 Elevate 5% Minoxidil Hair Liquid

5% Minoxidil

Hair regrowth treatment

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. (1-800-222-1222)

For external use only. For use on scalp only.
Avoid contact with eyes. Keep out of reach of children. Keep stored at room temperature.

Aqua, Propylene Glycol, 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.

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.

store at 20"to 25"(68 to 77F). Keep tightly closed.

-Prevent and Stop Hair Loss
-Stimulate Hair Growth
-Improve Fullness of Hair
-Restore Vitality of Hair
-Strengthen and Activate Hair Follicles

Elevate 5% Minoxidil
is applied to the scalp and used to stimulate hair
growth in adult men and women. It’s a spray
solution that’s been approved by the FDA to
treat hair loss and help regrow hair.

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.

ELEVATE 5% MINOXIDIL HAIR LIQUID 
elevate 5% minoxidil hair liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83830-103
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
COCONUT OIL (UNII: Q9L0O73W7L)	1 mL  in 100 mL
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)	0.5 mL  in 100 mL
GREEN TEA LEAF (UNII: W2ZU1RY8B0)	1 mL  in 100 mL
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)	0.5 mL  in 100 mL
1,2-HEXANEDIOL (UNII: TR046Y3K1G)	0.5 mL  in 100 mL
SARCOSINE (UNII: Z711V88R5F)	0.5 mL  in 100 mL
BIOTIN (UNII: 6SO6U10H04)	1 mL  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	35 mL  in 100 mL
PANTHENOL (UNII: WV9CM0O67Z)	5 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	40.95 mL  in 100 mL
FALLOPIA MULTIFLORA ROOT (UNII: AUZ3VD75MC)	0.5 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	5 mL  in 100 mL
GINGER (UNII: C5529G5JPQ)	3 mL  in 100 mL
NUTMEG (UNII: AEE24M3MQ9)	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: 83830-103-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/26/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/26/2023	03/07/2024

Labeler - Foshan Yilai Cosmetics Co., Ltd. (602056456)

Registrant - Foshan Yilai Cosmetics Co., Ltd. (602056456)

Establishment
Name	Address	ID/FEI	Business Operations
Foshan Yilai Cosmetics Co., Ltd.		602056456	manufacture(83830-103)

Revised: 3/2024

Document Id: 130e77f5-8bb3-7f26-e063-6294a90ae8dd

34390-5

Set id: 0d6192c9-a519-f6c2-e063-6294a90ab9bc

Version: 2

Effective Time: 20240307