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


label

PURE C SERUM 
niacinamide, adenosine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 70099-0004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 g  in 100 mL
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 70099-0004-130 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product12/29/201610/30/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/29/201610/30/2019
Labeler - R&L Co., Ltd. (689036771)
Registrant - R&L Co., Ltd. (689036771)
Establishment
NameAddressID/FEIBusiness Operations
R&L Co., Ltd.689036771manufacture(70099-0004) , pack(70099-0004) , label(70099-0004)
Establishment
NameAddressID/FEIBusiness Operations
CIT CO.,LTD690081646manufacture(70099-0004)

Revised: 10/2019
 
R&L Co., Ltd.