APPLICELL ADVANCED- dimethicone lotion 
Anc HnB Inc.

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 Ingredient: Dimethicone 3.5%

INACTIVE INGREDIENT

Inactive Ingredients: Water, Hydrogenated Polydecene, Triethylhexanoin, Butylene Glycol, Glycerin, Citrus Paradisi (Grapefruit) Fruit Extract, PEG-5 Glyceryl Stearate , PEG-100 Stearate, Glyceryl Stearate, Isostearic Acid, Stearic Acid, Macadamia Ternifolia Seed Oil, Betaine, Trehalose, Glyceryl Stearate SE, Behenic Acid, Behenyl Alcohol, Human fibroblast Conditioned Media, Neofinetia Falcata Callus Culture Extract, Phenoxyethanol, Fragrance, Carbomer, Portulaca Oleracea Extract, Hydrolyzed Keratin, Hydrolyzed Collagen, Hydrolyzed Elastin, Coix Lacryma-Jobi Ma-yuen Seed Extract, Potassium Hydroxide, Trisodium EDTA, Caprylhydroxamic Acid, Caprylyl Glycol

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 Advanced Lotion is available to nourish to the skin and brings a soft, moist feel.

DOSAGE & ADMINISTRATION

How to use: After serum, take proper amount and apply over the face along skin texture.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

APPLICELL ADVANCED 
dimethicone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71098-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Dimethicone (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) Dimethicone4.55 g  in 130 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71098-010-021 in 1 CARTON10/10/2016
1NDC:71098-010-01130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34710/10/2016
Labeler - Anc HnB Inc. (689031836)
Registrant - Anc HnB Inc. (689031836)
Establishment
NameAddressID/FEIBusiness Operations
Anc HnB Inc.689031836manufacture(71098-010)

Revised: 11/2016
Document Id: 9cbc4165-acc8-46ed-8a5a-95d68b3555a2
Set id: 7909a2df-88f0-41f9-aa4e-42bdddf2db45
Version: 1
Effective Time: 20161125
 
Anc HnB Inc.