SUBIR EYELASH- setting 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.

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Active Ingredient(s)

Sodium Bromate 12%

Purpose

For permanent wave

Use

Subir Eyelash Setting Cream for eyelash permanent wave

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

• After desired time has passed, remove perm cream (step1). Use a newly moistened cotton pad to remove all traces of perm cream (step1)
• Follow the same application technique to apply setting cream(step2), as you did to (step1).
• After removing the perm cream, apply the setting cream and after 10 ~ 12 minutes, remove the set cream using a newly moistened cotton pad (depending on the texture of the lashes).

Other information

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

Inactive ingredients

Water, PolyPropyleneGlycol-7, Cetearyl Alcohol, Mineral Oil, Cetyl Alcohol, Stearyl Alcohol

Package Label - Principal Display Panel

image description

SUBIR EYELASH 
setting cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81716-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STRONTIUM BROMATE (UNII: 1T54WJB20V) (STRONTIUM BROMATE - UNII:1T54WJB20V) STRONTIUM BROMATE0.084 g  in 0.7 g
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Cetyl Alcohol (UNII: 936JST6JCN)  
Stearyl Alcohol (UNII: 2KR89I4H1Y)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81716-003-010.7 g in 1 POUCH; Type 0: Not a Combination Product03/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/31/2021
Labeler - Dream Polymer (695501990)
Registrant - Dream Polymer (695501990)
Establishment
NameAddressID/FEIBusiness Operations
Dream Polymer695501990manufacture(81716-003)

Revised: 3/2021
Document Id: ffd4eecd-51ba-4ff3-9828-f29b2b4cce81
Set id: aa189b1a-ce65-4896-a14d-7e8a8546a624
Version: 1
Effective Time: 20210331
 
Dream Polymer