RENEW PEELING PAD- adenosine liquid 
Racce 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: Adenosine 0.04%

INACTIVE INGREDIENT

Inactive ingredients: Water, Dipropylene Glycol, Glycerine, Houttuynia Cordata Extract, Arginine, Aloe Barbadensis Leaf Powder, Portulaca Oleracea Extract, Salvia Officinalis (Sage) Leaf Extract, Origanum Vulgare Leaf Extract, Polysorbate 20, Allantoin, 1,2-Hexanediol, Kappaphycus alvarezii Extract/Caesalpinia spinosa Fruit Extract, Glycolic Acid, Adenosine, Malva Sylvestris (Mallow) Extract,Mentha Piperita (Peppermint) Leaf Extract, Primula Veris Extract, Alchemilla Vulgaris Extract, Veronica Officinalis Extract, Melissa Officinalis Leaf Extract, Achillea Millefolium Extract, Sodium Hydroxide

PURPOSE

Purpose: Anti wrinkle

WARNINGS

Warnings: For external use only. Avoid contact with eyes: If contact or irritation develops, discontinue use and consult a dermatologist. Away from children.

KEEP OUT OF REACH OF CHILDREN

Away from children.

Uses

Uses:

- supports skin’s firmness and maximizes bright radiance

- Improves dryness and dullness of the skin and helps look fresher and renewed.

Directions

Directions:

Step1: Wipe over the face to remove dirt and impuiries. No need to rinse after use

Step2: Stretch the mask on the face and then leave on for 10-15minutes. Remove mask pad and lightly massage. Use once or twice a week or as needed.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

RENEW PEELING PAD 
adenosine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72092-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine0.002 g  in 6 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Dipropylene Glycol (UNII: E107L85C40)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72092-010-025 in 1 CARTON01/02/201812/01/2018
1NDC:72092-010-016 mL in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/02/201812/01/2018
Labeler - Racce Co., Ltd. (694890309)
Registrant - Racce Co., Ltd. (694890309)
Establishment
NameAddressID/FEIBusiness Operations
Racce Co., Ltd.694890309manufacture(72092-010)

Revised: 3/2019
 
Racce Co., Ltd.