FORESTHEAL WHIPPING FOA M CLEANSER- niacinamide liquid 
BONNE 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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ACTIVE INGREDIENT

Active ingredients: NIACINAMIDE 2.0%

INACTIVE INGREDIENT

Inactive ingredients:

Water, Glycerin, Palmitic Acid, Lauric Acid, Stearic acid, Potassium Hydroxide, Myristic Acid, Potassium Cocoyl Glycinate, Disodium Cocoamphodiacetate, Glyceryl Stearate, PEG-100 Stearate, Beeswax, Sorbitan Olivate, Glycol Distearate, Cocamidopropyl Betaine, Polysorbate 60, Sodium Chloride, Phenoxyethanol, Fragrance, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Hydroxyethylcellulose, Ethylhexylglycerin, PEG-90M, Polyquaternium-7, Disodium EDTA, Hexylene Glycol, Carapa Guaianensis Seed Oil, Sodium Benzoate, Silica, Betaine, Allantoin, Carica Papaya (Papaya) Fruit Extract, 1,2-Hexanediol, Sodium Hyaluronate

PURPOSE

Purpose: Skin Brightening

WARNINGS

Warnings:

• Do not use on damaged or broken skin.

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

• Do not use while pregnancy.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Uses

Uses:

Helps brighten the skin tone.

Directions

Directions:

Take an appropriate amount of foam and massage the entire face gently, then rinse thoroughly with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

FORESTHEAL WHIPPING FOA M CLEANSER 
niacinamide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69997-190
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE3.60 g  in 180 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69997-190-021 in 1 CARTON03/01/201806/29/2018
1NDC:69997-190-01180 mL in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/01/201806/29/2018
Labeler - BONNE CO.,LTD (557821750)
Registrant - BONNE CO.,LTD (557821750)
Establishment
NameAddressID/FEIBusiness Operations
HANACOS CO., LTD.690177857manufacture(69997-190)

Revised: 7/2018
Document Id: 97be0ba6-44c3-4acf-9ff4-bce04cb312fe
Set id: a5280944-39ff-4ee5-97fb-f6d33ac8111b
Version: 3
Effective Time: 20180709
 
BONNE CO.,LTD