NDC 43596-0078 Cy Bb Facial Hidratante Con Color Fps 25 Multibeneficios
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What is NDC 43596-0078?
What are the uses for Cy Bb Facial Hidratante Con Color Fps 25 Multibeneficios?
Which are Cy Bb Facial Hidratante Con Color Fps 25 Multibeneficios UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Cy Bb Facial Hidratante Con Color Fps 25 Multibeneficios 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- 4-HYDROXY ACETOPHENONE (UNII: G1L3HT4CMH)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- SILANEDIOL SALICYLATE (UNII: C054DF30K0)
- TROMETHAMINE (UNII: 023C2WHX2V)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- COCOA (UNII: D9108TZ9KG)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".