PURIFYING RELIEF SOOTHING GEL ESSENCE- niacinamide, adenosine liquid

purifying relief soothing gel essence by

Drug Labeling and Warnings

purifying relief soothing gel essence by is a Otc medication manufactured, distributed, or labeled by In This Morning. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

niacinamide, adenosine

INACTIVE INGREDIENT

water, butylene glycol, etc.

PURPOSE

skin brightening, alleviate wrinkles

KEEP OUT OF REACH OF CHILDREN

keep out or reach of the children

INDICATIONS & USAGE

apply moderate amount of this product evenly on the face until absorbed

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

PURIFYING RELIEF SOOTHING GEL ESSENCE 
niacinamide, adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71217-0039
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
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g  in 100 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: 71217-0039-1	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/26/2019

Labeler - In This Morning (694519423)

Registrant - In This Morning (694519423)

Establishment
Name	Address	ID/FEI	Business Operations
In This Morning		694519423	label(71217-0039) , pack(71217-0039) , manufacture(71217-0039)