APPLICELL ESSENTIAL TONER- adenosine liquid

Applicell Essential Toner by

Drug Labeling and Warnings

Applicell Essential Toner 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: Adenosine 0.04%

INACTIVE INGREDIENT

Inactive Ingredients: Water, Alcohol, Sodium Hyaluronate, Portulaca Oleracea Extract, Hydrolyzed Keratin, Hydrolyzed Collagen, Hydrolyzed Elastin, Betaine, Trehalose, Citrus Paradisi (Grapefruit) Fruit Extract, Methyl Gluceth-20, Caprylhydroxamic Acid, Caprylyl Glycol, Human fibroblast Conditioned Media, PEG-40 Hydrogenated Castor Oil, Neofinetia Falcata Callus Culture Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Xanthan Gum, Potassium Hydroxide, Phenoxyethanol, 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 Essential Toner is the wrinkle functional toner that provides moisture, a silky feel and nourishment to the skin.

DOSAGE & ADMINISTRATION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

APPLICELL ESSENTIAL TONER 
adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71098-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	Adenosine	0.05 g  in 130 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Alcohol (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71098-020-02	1 in 1 CARTON	10/10/2016
1	NDC: 71098-020-01	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
unapproved drug other		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(71098-020)