TERADIA THE LIQUIDDIAMOND SUNSCREEN SPF50- ethylhexyl methoxycinnamate, homosalate, ethylhexyl salicylate cream 
NanoDia Lab Co Ltd

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Octinoxate, Homosalate, Octisalate

Niacinamide, Adenosine

Sunscreen, Anti-Wrinkle, Whitening

keep out of reach of the children

At the last step of skin care, take an appropriate amount and apply evenly on the face, neck and other areas exposed to UV radiation

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

TERADIA THE LIQUIDDIAMOND SUNSCREEN SPF50 
ethylhexyl methoxycinnamate, homosalate, ethylhexyl salicylate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71483-0001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE6 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ADENOSINE (UNII: K72T3FS567)  
NIACINAMIDE (UNII: 25X51I8RD4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71483-0001-140 mL in 1 TUBE; Type 0: Not a Combination Product12/20/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35212/20/2017
Labeler - NanoDia Lab Co Ltd (693900835)
Registrant - NanoDia Lab Co Ltd (693900835)
Establishment
NameAddressID/FEIBusiness Operations
NanoDia Lab Co Ltd693900835manufacture(71483-0001)

Revised: 12/2018
Document Id: 7d58538d-f1d1-abaf-e053-2a91aa0ae2f1
Set id: 60e74fb5-d4b8-79a0-e053-2a91aa0a4eed
Version: 3
Effective Time: 20181218
 
NanoDia Lab Co Ltd