NDC 69888-103 Primerose White Milky Cb
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 69888-103?
Which are Primerose White Milky Cb UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are Primerose White Milky Cb 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- MACADAMIA OIL (UNII: 515610SU8C)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GLYCERIN (UNII: PDC6A3C0OX)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- CETYL DIMETHICONE 45 (UNII: IK315POC44)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- SQUALANE (UNII: GW89575KF9)
- CERAMIDE 3 (UNII: 4370DF050B)
- SHEA BUTTER (UNII: K49155WL9Y)
- BETAINE (UNII: 3SCV180C9W)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ALLANTOIN (UNII: 344S277G0Z)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
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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".