DR VITA PREMIUM VITAMIN C- dimethicone cream
DAYCELL COSMETICS 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.

----------

ACTIVE INGREDIENT

Active Ingredient: DIMETHICONE 3.0%

INACTIVE INGREDIENT

Inactive Ingredients: GLYCERIN, PROPYLENE GLYCOL, CYCLOMETHICONE, ASCORBIC ACID, CYCLOPENTASILOXANE, PEG/PPG-18/18 DIMETHICONE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, DIMETHICONE, CENTELLA ASIATICA EXTRACT, FICUS CARICA (FIG) FRUIT EXTRACT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, HYDROGENATED LECITHIN, 1,2-HEXANEDIOL, PEG/PPG-19/19 DIMETHICONE, ETHYLHEXYLGLYCERIN, ADENOSINE, HYDROGENATED PHOSPHATIDYLCHOLINE, RETINOL, CERAMIDE NP, CHOLESTEROL, CETYL ALCOHOL, STEARYL ALCOHOL, FRAGRANCE, PHENOXYETHANOL

PURPOSE

Purpose: Brightening & wrinkle care

WARNINGS

Warnings: Avoid application to wounded or infected area. Do NOT use if irritation develops. If so, consult a physician immediately. Keep out of reach of children. Cover lid after each use. Store at a cool, dry place, away from direct sunlight.

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

Indications & Usage: 1. After vitamin mask pack, put size of a nickel on the palm and apply to troubled areas, entire face, or neck evenly. 2. For the face, apply outwards and top-down for the neck.

DOSAGE & ADMINISTRATION

Dosage & Administration: Everyday night

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

DR VITA PREMIUM VITAMIN C
dimethicone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70545-020
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	0.9 g in 30 g

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:70545-020-01	30 g in 1 CARTON; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	02/01/2016

Labeler - DAYCELL COSMETICS CO., LTD. (688289734)

Registrant - DAYCELL COSMETICS CO., LTD. (688289734)

Name	Address	ID/FEI	Business Operations
Establishment
DAYCELL COSMETICS CO., LTD.		688289734	manufacture(70545-020)