NDC 69888-102 Primerose Egf
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69888 - Royal Springs Cosmetics Usa, Llc
- 69888-102 - Primerose Egf
Product Packages
NDC Code 69888-102-02
Package Description: 1 CONTAINER in 1 BOX / 100 mL in 1 CONTAINER (69888-102-01)
Product Details
What is NDC 69888-102?
Which are Primerose Egf UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are Primerose Egf 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)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- MACADAMIA OIL (UNII: 515610SU8C)
- ARGININE (UNII: 94ZLA3W45F)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- POMEGRANATE (UNII: 56687D1Z4D)
- CARAMEL (UNII: T9D99G2B1R)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- AMYLOPECTIN (UNII: 4XO4QFV777)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- EDETATE SODIUM (UNII: MP1J8420LU)
* 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".