APPLICELL PERFECT EYE- adenosine cream 
Anc HnB Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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ACTIVE INGREDIENT

Active Ingredient: Adenosine 0.04%

INACTIVE INGREDIENT

Inactive Ingredients: Water, Glycerin, Dipropylene Glycol, Hydrogenated Polydecene, Cyclopentasiloxane, Cyclohexasiloxane, Hydrolyzed Keratin, Hydrolyzed Collagen, Hydrolyzed Elastin, Cetearyl Alcohol, Polyglyceryl-3 Methylglucose Distearate, Betaine, Butyrospermum Parkii(Shea Butter), Neopentyl Glycol Dicaprate, Dimethicone, Triethylhexanoin, Glyceryl Stearate SE, Sodium Hyaluronate, Human fibroblast Conditioned Media, Stearic Acid, Beeswax, PEG-100 Stearate, Citrus Paradisi (Grapefruit) Fruit Extract, Glyceryl Stearate, Tocopheryl Acetate, Xanthan Gum, Ceramide 3, Hydrogenated Lecithin, Neofinetia Falcata Callus Culture Extract, Caprylhydroxamic Acid, Caprylyl Glycol, Phenoxyethanol, Carbomer, Potassium Hydroxide, Trisodium EDTA, Fragrance

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warnings: For external use only When using this product do not get into eyes, Stop use and ask a doctor if rash occurs Do not use on - deep puncture wounds - animal bites - serious burns Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

Indications & usage: APPLICELL Perfect Eye Cream will moist and elastically care for wrinkle around the eyes.

DOSAGE & ADMINISTRATION

How to use: Apply around the eye area after Serum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

APPLICELL PERFECT EYE 
adenosine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71098-050
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine0.01 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71098-050-021 in 1 CARTON10/10/2016
1NDC:71098-050-0130 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/10/2016
Labeler - Anc HnB Inc. (689031836)
Registrant - Anc HnB Inc. (689031836)
Establishment
NameAddressID/FEIBusiness Operations
Anc HnB Inc.689031836manufacture(71098-050)

Revised: 11/2016
Document Id: ae64797c-dbf0-4299-8aea-6b8810f0d217
Set id: 60bf611d-22a2-483e-b6f7-c4f50797d55f
Version: 1
Effective Time: 20161125
 
Anc HnB Inc.