Pure C Serum by R&L Co., Ltd. / CIT CO.,LTD Drug Facts

Pure C Serum by

Drug Labeling and Warnings

Pure C Serum by is a Otc medication manufactured, distributed, or labeled by R&L Co., Ltd., CIT CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURE C SERUM- niacinamide, adenosine liquid 
R&L Co., Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

Niacinamide, Adenosine

Water, Butylene Glycol, etc.

Skin Protect

keep out of reach of the children

• Apply a small amount on clean skin each morning and night.
• avoiding eye area.
• May be used before using the Rejuvena PREMIUM in G-Blue and G-Red mod.

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

for external use only

PURE C SERUM 
niacinamide, adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70099-0004
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
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70099-0004-1	30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	12/29/2016	10/30/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/29/2016	10/30/2019

Labeler - R&L Co., Ltd. (689036771)

Registrant - R&L Co., Ltd. (689036771)

Establishment
Name	Address	ID/FEI	Business Operations
R&L Co., Ltd.		689036771	manufacture(70099-0004) , pack(70099-0004) , label(70099-0004)

Establishment
Name	Address	ID/FEI	Business Operations
CIT CO.,LTD		690081646	manufacture(70099-0004)

Revised: 10/2019

Document Id: 9619aeb7-884a-2518-e053-2a95a90afa4a

34390-5

Set id: 44c258e6-9c6a-56f2-e054-00144ff8d46c

Version: 2

Effective Time: 20191029

 

R&L Co., Ltd.