SUBIR EYELASH- biotin cream

SUBIR EYELASH by

Drug Labeling and Warnings

SUBIR EYELASH by is a Otc medication manufactured, distributed, or labeled by Dream Polymer. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Biotin 10%

D-Panthenol 8%

Purpose

Anti-static, Hair conditioning, Skin conditioning

Use

Subir Eyelash Biotin Cream for eyelash damage care

Warnings

Be careful not to get in your eyes.
If it gets into your eyes, immediately wash it off with clean water several times.
Wear appropriate gloves during the procedure.
Do not eat.
Keep out of reach of children.
Store in a cool place away from direct sunlight.
Recommended for single use only.
For professional use only.
Follow the recommendations.
After use, if skin irritation such as rash or itching persists, stop use and consult a doctor or pharmacist

KEEP OUT OF REACH OF CHILDREN

 Keep out of reach of children.

Directions

Using a Brush follow the same steps used for applying the perm and setting creams to applying the Essence (nourishing agent).
Let nourishing set for five minutes.
Prevents eyelash damage and promotes growth.

Other information

・ Store in room temperature 0~30℃
・ Avoid direct sunlight.

Inactive ingredients

Water, Propylene Glycol(PG), Acrus Calamus Rhizome Oil, Aloe Barbadensis (Aloe Vera) Leaf Juice, Chamaecyparis Obtusa Leaf Extract, Olea Europaea (Olive) Leaf Extract, Espinosilla Extract, Decametyl Tetra Siloxane, Fragrance

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

SUBIR EYELASH 
biotin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81716-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04)	BIOTIN	0.07 g  in 0.7 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Propylene Glycol (UNII: 6DC9Q167V3)
OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81716-004-01	0.7 g in 1 POUCH; Type 0: Not a Combination Product	03/30/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/30/2021

Labeler - Dream Polymer (695501990)

Registrant - Dream Polymer (695501990)

Establishment
Name	Address	ID/FEI	Business Operations
Dream Polymer		695501990	manufacture(81716-004)