BIOTOC REGEN AMPOULE- adenosine liquid

Biotoc Regen Ampoule by

Drug Labeling and Warnings

Biotoc Regen Ampoule by is a Otc medication manufactured, distributed, or labeled by Dermafirm INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Adenosine

INACTIVE INGREDIENT

Water, Glycerin

PURPOSE

Anti-Wrinkle

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

After toning or at ther toner step, drop the appropriate amount of Biotoc Regen Ampoule on your face (apply first on deep lines) and let it absorb by tapping lightly.

Using Biotoc line before makeup, you can get smooth and shining look.

WARNINGS

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BIOTOC REGEN AMPOULE 
adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71638-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.04 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71638-0001-1	100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/04/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/04/2017

Labeler - Dermafirm INC. (690171603)

Registrant - Dermafirm INC. (690171603)

Establishment
Name	Address	ID/FEI	Business Operations
Dermafirm INC.		690171603	label(71638-0001) , pack(71638-0001) , manufacture(71638-0001)