APPLICELL ADVANCED- dimethicone lotion

Applicell Advanced by

Drug Labeling and Warnings

Applicell Advanced by is a Otc medication manufactured, distributed, or labeled by Anc HnB Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

APPLICELL ADVANCED 
dimethicone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71098-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Dimethicone (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	Dimethicone	4.55 g  in 130 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71098-010-02	1 in 1 CARTON	10/10/2016
1	NDC: 71098-010-01	130 mL in 1 BOTTLE, PUMP; 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	10/10/2016

Labeler - Anc HnB Inc. (689031836)

Registrant - Anc HnB Inc. (689031836)

Establishment
Name	Address	ID/FEI	Business Operations
Anc HnB Inc.		689031836	manufacture(71098-010)