FILLIZER MADHUCA AMPOULE- salicylic acid, tocopheryl acetate, niacinamide liquid 
CJ ENM 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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Drug Facts

salicylic acid, tocopheryl acetate, niacinamide

antiseptic

KEEP OUT OF REACH OF THE CHILDREN

apply proper amount to the subject area

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

for external use only

Water
Alcohol
Polysorbate 80
Benzyl Glycol
Ammonium Acryloyldimethyltaurate/VP Copolymer
Avena Sativa (Oat) Leaf Extract
Trideceth-10
Salicylic Acid
Butylene Glycol
Madhuca Longifolia Sophorolipids(0.8%)
Fragrance
Hydrolyzed Collagen
Citrus Unshiu Peel Extract
Dipotassium Glycyrrhizate
Sodium Citrate
Ethylhexylglycerin
Pyridoxine HCl
1,2-Hexanediol
Raspberry Ketone
Menthol
Althaea Rosea Flower Extract
Coffea Arabica (Coffee) Seed Extract
Camellia Sinensis Leaf Extract
Morus Alba Bark Extract
Perilla Frutescens Leaf Extract
Houttuynia Cordata Extract
Polygonum Multiflorum Root Extract
Limonene
Geraniol
Citronellol
Butylphenyl Methylpropional
Linalool
Alpha-Isomethyl Ionone
Hydroxycitronellal
Amyl Cinnamal
Benzyl Benzoate
Citral

label

FILLIZER MADHUCA AMPOULE 
salicylic acid, tocopheryl acetate, niacinamide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81069-0001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1) .ALPHA.-TOCOPHEROL ACETATE2 g  in 100 mL
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.495 g  in 100 mL
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81069-0001-17.5 mL in 1 BOTTLE; Type 0: Not a Combination Product11/14/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/14/2020
Labeler - CJ ENM Co., Ltd. (687982736)
Registrant - CJ ENM Co., Ltd. (687982736)
Establishment
NameAddressID/FEIBusiness Operations
CJ ENM Co., Ltd.687982736manufacture(81069-0001) , label(81069-0001)

Revised: 11/2020
Document Id: b406f778-e3c1-2766-e053-2a95a90a8383
Set id: b406f41a-5a81-762d-e053-2995a90a064c
Version: 1
Effective Time: 20201113
 
CJ ENM Co., Ltd.