Label: DR.PLINUS FILLINCELL MULTI EX- niacinamide, adenosine patch
-
Contains inactivated NDC Code(s)
NDC Code(s): 72630-040-01, 72630-040-02, 72630-040-03 - Packager: S Skin Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated November 21, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- INACTIVE INGREDIENTS
- PURPOSE
-
WARNINGS
1. Discontinue to use or consult with dermatologist if irritation, swelling or itching appears after applying the product
2. Avoid applying patches on the wounded, dermatitis, and inflamed skin parts
3. Safety and storage precautions
A) Keep out of children's reach
B) Keep away from direct sunlight
C) Use immediately after opening
D) Do not reuse the patch you have already attached once
E) For external use only - KEEP OUT OF REACH OF CHILDREN
- Uses
-
Directions
① Before using the patch, wash your face.
② Open the pouch and take the patches out from the clear case, and remove the protective films on patch
(* one by one. At this point, be careful not to touch the middle part of the patch.)
③ Adjust the patches on your face where you concern and press lightly at a right angle.
④ Attach the patch above at least 60 minutes. - Other Information
- QUESTIONS
- NDC#: 72630-040-02DR.PLINUS FILLINCELL MULTI PATCH EX (POUCH)
- NDC#: 72630-040-03DR.PLINUS FILLINCELL MULTI PATCH EX (BOX)
-
INGREDIENTS AND APPEARANCE
DR.PLINUS FILLINCELL MULTI EX
niacinamide, adenosine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72630-040 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.006 g in 0.3 g Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.00012 g in 0.3 g Inactive Ingredients Ingredient Name Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72630-040-02 2 in 1 POUCH 11/01/2022 1 NDC:72630-040-01 0.3 g in 1 PATCH; Type 0: Not a Combination Product 2 NDC:72630-040-03 8 in 1 BOX 11/01/2022 2 NDC:72630-040-01 0.3 g in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/01/2022 Labeler - S Skin Co., Ltd. (694879753) Registrant - S Skin Co., Ltd. (694879753) Establishment Name Address ID/FEI Business Operations BIOCOSONE CO.,LTD 695729438 manufacture(72630-040)