ULTRA V RENEWDERM PLUS- dimethicone cream

Ultra V RENEWDERM PLUS by

Drug Labeling and Warnings

Ultra V RENEWDERM PLUS by is a Otc medication manufactured, distributed, or labeled by Ultra V Co., Ltd, NEW & NEW CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

ULTRA V RENEWDERM PLUS 
dimethicone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71975-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Dimethicone (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	Dimethicone	3.81 g  in 50 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71975-010-02	1 in 1 CARTON	01/02/2018
1	NDC: 71975-010-01	50 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	01/02/2018

Labeler - Ultra V Co., Ltd (689004748)

Registrant - Ultra V Co., Ltd (689004748)

Establishment
Name	Address	ID/FEI	Business Operations
NEW & NEW CO.,LTD.		557821160	manufacture(71975-010)