NDC 76173-1004 The Cellin Eop B.b Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 76173-1004?
What are the uses for The Cellin Eop B.b Cream?
Which are The Cellin Eop B.b Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are The Cellin Eop B.b Cream 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- TALC (UNII: 7SEV7J4R1U)
- ARBUTIN (UNII: C5INA23HXF)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- PORTULACA OLERACEA WHOLE (UNII: D5J3623SV2)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- PALMITIC ACID (UNII: 2V16EO95H1)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ADENOSINE (UNII: K72T3FS567)
- NIACINAMIDE (UNII: 25X51I8RD4)
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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".