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NDC 72630-0020-02 DR.PLINUS FILLINCELL MULTI .0002; .21; .007 g/.3g; g/.3g; g/.3g Details

DR.PLINUS FILLINCELL MULTI .0002; .21; .007 g/.3g; g/.3g; g/.3g

DR.PLINUS FILLINCELL MULTI is a TOPICAL PATCH in the HUMAN OTC DRUG category. It is labeled and distributed by S Skin Co., Ltd.. The primary component is ADENOSINE; HYALURONATE SODIUM; NIACINAMIDE.

Product Information

NDC	72630-0020
Product ID	72630-020_6c5a6ea1-c140-46c2-bea1-2f1cb2f3d582
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	DR.PLINUS FILLINCELL MULTI
Proprietary Name Suffix	n/a
Non-Proprietary Name	Sodium Hyaluronate, Niacinamide, Adenosine
Product Type	HUMAN OTC DRUG
Dosage Form	PATCH
Route	TOPICAL
Active Ingredient Strength	.0002; .21; .007
Active Ingredient Units	g/.3g; g/.3g; g/.3g
Substance Name	ADENOSINE; HYALURONATE SODIUM; NIACINAMIDE
Labeler Name	S Skin Co., Ltd.
Pharmaceutical Class	Adenosine Receptor Agonist [EPC], Adenosine Receptor Agonists [MoA]
DEA Schedule	n/a
Marketing Category	UNAPPROVED DRUG OTHER
Application Number	n/a
Listing Certified Through	2023-12-31

Package

Package Images

NDC 72630-0020-02 (72630002002)

Pricing Information	N/A
NDC Package Code	72630-020-02
Billing NDC	72630002002
Package	2 PATCH in 1 CONTAINER (72630-020-02) / .3 g in 1 PATCH (72630-020-01)
Marketing Start Date	2021-05-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 1d6da6f7-bcc4-4efc-a8b1-9b80bedd85af Details

ACTIVE INGREDIENTS

Sodium Hyaluronate 70.05%

Niacinamide 2.45%

Adenosine 0.08%

INACTIVE INGREDIENTS

Water, Propanediol, Glycerin, Butylene Glycol, Diglucosyl Gallic Acid, Hydrolyzed Vegetable Protein, Adenosine Triphosphate, Sodium Chondroitin Sulfate, Anogeissus Leiocarpus Bark Extract, Epigallocatechin Gallatyl Glucoside

PURPOSE

Moisture

Skin Brightening

Anti wrinkle

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

Keep out of children's reach

Uses

■ Helps moisturize your skin

■ Helps brighten skin tone

■ Helps improve wrinkle problem

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

■ Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light

QUESTIONS

■ https://www.drplinus.com/ +82.1811.8665

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.PLINUS FILLINCELL MULTI

sodium hyaluronate, niacinamide, adenosine patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:72630-020
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONATE SODIUM	0.21 g in 0.3 g
Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	Niacinamide	0.007 g in 0.3 g
Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	Adenosine	0.0002 g in 0.3 g

Ingredient Name	Strength
Inactive Ingredients
Water (UNII: 059QF0KO0R)
Propanediol (UNII: 5965N8W85T)
Glycerin (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:72630-020-02	2 in 1 CONTAINER	05/01/2021
1	NDC:72630-020-01	0.3 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		05/01/2021

Labeler - S Skin Co., Ltd. (694879753)

Registrant - S Skin Co., Ltd. (694879753)

Name	Address	ID/FEI	Business Operations
Establishment
BIOCOSONE CO.,LTD		695729438	manufacture(72630-020)

Revised: 10/2022

Document Id: 6c5a6ea1-c140-46c2-bea1-2f1cb2f3d582

Set id: 1d6da6f7-bcc4-4efc-a8b1-9b80bedd85af

Version: 2

Effective Time: 20221018