ULTRA V RENEWDERM PLUS- dimethicone cream 
Ultra V Co., Ltd

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ACTIVE INGREDIENT

Active ingredients: Dimethicone 7.63%

INACTIVE INGREDIENT

Inactive ingredients: Water, Glycerin, Cyclopentasiloxane, Butylene Glycol, Centella Asiatica Extract, Cyclohexasiloxane, Arbutin , Alcohol , PEG/PPG-19/19 Dimethicone, Beta-Glucan , Biosaccharide Gum-1 , Piper Methysticum Leaf/Root/Stem Extract, Dimethicone/Vinyl Dimethicone Crosspolymer , Glycyrrhiza Glabra (Licorice) Root Extract, Dipotassium Glycyrrhizate, Phellinus Linteus Extract , Phenoxyethanol, Methylparaben, Betaine , Acetyl Hexapeptide-8, Copper Tripeptide-1 , Palmitoyl Oligopeptide, Palmitoyl Tetrapeptide-7, rh-Oligopeptide-1, Sodium Metabisulfite, Glyceryl Acrylate/Acrylic Acid Copolymer, Disodium EDTA, Benzophenone-9, Fragrance, Propylene Glycol, Sodium Hyaluronate

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warnings: For external use only. Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use. Keep out of reach of children.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Uses

Uses: Helps protect skin

Directions

Directions: After facial wash, apply an adequate amount on face and neck. Apply twice a day on normal skin, morning and night, at the last stage of skin care. Tap gently for max absorption.

QUESTIONS

Questions:

TEL,+82-539-3450

www.ultravcosmetic.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

ULTRA V RENEWDERM PLUS 
dimethicone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71975-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Dimethicone (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) Dimethicone3.81 g  in 50 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71975-010-021 in 1 CARTON01/02/2018
1NDC:71975-010-0150 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34701/02/2018
Labeler - Ultra V Co., Ltd (689004748)
Registrant - Ultra V Co., Ltd (689004748)
Establishment
NameAddressID/FEIBusiness Operations
NEW & NEW CO.,LTD.557821160manufacture(71975-010)

Revised: 4/2020
Document Id: e794e32a-a7b2-4438-bafe-b9cb2fb462f0
Set id: e7a5780b-816e-4a55-a1c1-955f9b49bfbd
Version: 2
Effective Time: 20200401
 
Ultra V Co., Ltd