Label: DR.PLINUS ZERO TROUBLE- gluconolactone, epigallocatechin gallatyl glucoside, madecassoside patch
- NDC Code(s): 72630-030-01, 72630-030-02
- Packager: S Skin Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated October 18, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- INACTIVE INGREDIENTS
- PURPOSE
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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
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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
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DR.PLINUS ZERO TROUBLE
gluconolactone, epigallocatechin gallatyl glucoside, madecassoside patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72630-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLUCONOLACTONE (UNII: WQ29KQ9POT) (GLUCONOLACTONE - UNII:WQ29KQ9POT) GLUCONOLACTONE 0.029 mg in 1.4 mg EPIGALLOCATECHIN GALLATYL GLUCOSIDE (UNII: AR8RR3M6N9) (EPIGALLOCATECHIN GALLATYL GLUCOSIDE - UNII:AR8RR3M6N9) EPIGALLOCATECHIN GALLATYL GLUCOSIDE 0.0007 mg in 1.4 mg Madecassoside (UNII: CQ2F5O6YIY) (Madecassoside - UNII:CQ2F5O6YIY) Madecassoside 0.00001 mg in 1.4 mg Inactive Ingredients Ingredient Name Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72630-030-02 9 in 1 CONTAINER 05/01/2021 1 NDC:72630-030-01 1.4 mg 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 05/01/2021 Labeler - S Skin Co., Ltd. (694879753) Registrant - S Skin Co., Ltd. (694879753) Establishment Name Address ID/FEI Business Operations BIOCOSONE CO.,LTD 695729438 manufacture(72630-030)