NDC 14783-035 Lbel Paris Regression Jour
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 14783-035?
What are the uses for Lbel Paris Regression Jour?
Which are Lbel Paris Regression Jour UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Lbel Paris Regression Jour 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)
- SOYBEAN (UNII: L7HT8F1ZOD)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- SNOW PEA (UNII: 84SKC33B1I)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MANNITOL (UNII: 3OWL53L36A)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TROLAMINE (UNII: 9O3K93S3TK)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SORBIC ACID (UNII: X045WJ989B)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- YEAST (UNII: 3NY3SM6B8U)
- ETHYLPARABEN (UNII: 14255EXE39)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
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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".