NDC 70326-102 Plalab Placenta Ample Essence
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70326 - Renocell Co., Ltd
- 70326-102 - Plalab Placenta Ample Essence
Product Packages
NDC Code 70326-102-02
Package Description: 1 BOTTLE, PUMP in 1 PACKAGE / 50 mL in 1 BOTTLE, PUMP (70326-102-01)
Product Details
What is NDC 70326-102?
Which are Plalab Placenta Ample Essence UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are Plalab Placenta Ample Essence Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8)
- HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- BETAINE (UNII: 3SCV180C9W)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897)
- POLYISOBUTYLENE (1300 MW) (UNII: 241BN7J12Y)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- THEANINE (UNII: 8021PR16QO)
- COW MILK FAT (UNII: 463JZS0XJ3)
- GLUTATHIONE (UNII: GAN16C9B8O)
- ZANTHOXYLUM PIPERITUM FRUIT PULP (UNII: 7PFC2VA251)
- PULSATILLA KOREANA ROOT (UNII: FY35I16MPL)
- USNEA BARBATA (UNII: D6DVA9TCAP)
- PROPANEDIOL (UNII: 5965N8W85T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- STAR ANISE FRUIT (UNII: CK15HA8438)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- XANTHAN GUM (UNII: TTV12P4NEE)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".