NDC 70912-100 White Lie
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 70912-100?
What are the uses for White Lie?
Which are White Lie UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
Which are White Lie 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:
- SODIUM ACRYLATE (UNII: 7C98FKB43H)
- USNEA BARBATA (UNII: D6DVA9TCAP)
- ZANTHOXYLUM PIPERITUM FRUIT PULP (UNII: 7PFC2VA251)
- PULSATILLA KOREANA WHOLE (UNII: 5R35881OBK)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- GLYCERIN (UNII: PDC6A3C0OX)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
- ZINGIBER OFFICINALE WHOLE (UNII: IN6Q3S3414)
- SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)
- COPTIS CHINENSIS ROOT (UNII: CXS4LJR7EL)
- NEPIDERMIN (UNII: TZK30RF92W)
- ASIATICOSIDE (UNII: PKO39VY215)
- PEG-60 CASTOR OIL (UNII: VXP26NM2XX)
- AZADIRACHTA INDICA LEAF (UNII: HKY915780T)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- TARAXACUM OFFICINALE LEAF (UNII: 0022LFJ74Y)
- ARTEMISIA ANNUA LEAF (UNII: E4M09UY5BL)
- SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)
- HELICHRYSUM ARENARIUM WHOLE (UNII: OI6T8BMF4T)
- ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13)
- RHODIOLA ROSEA ROOT (UNII: 3S5ITS5ULN)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
* Please review the disclaimer below.
[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".