SUBIR EYELASH- biotin cream 
Dream Polymer

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.

----------

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.

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

image description

SUBIR EYELASH 
biotin cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81716-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) BIOTIN0.07 g  in 0.7 g
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Propylene Glycol (UNII: 6DC9Q167V3)  
OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)  
CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81716-004-010.7 g in 1 POUCH; Type 0: Not a Combination Product03/30/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/30/2021
Labeler - Dream Polymer (695501990)
Registrant - Dream Polymer (695501990)
Establishment
NameAddressID/FEIBusiness Operations
Dream Polymer695501990manufacture(81716-004)

Revised: 3/2021
Document Id: a0dc6a50-290e-452a-9928-2a0a215df7a4
Set id: 5fd088e3-4e49-4a04-b636-31ac0c22a1b8
Version: 1
Effective Time: 20210330
 
Dream Polymer