NDC 43596-0003 Lbel Regression Jour Protective Complex With Spf 15 Facial Day Normal To Combination Skin
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 43596-0003?
What are the uses for Lbel Regression Jour Protective Complex With Spf 15 Facial Day Normal To Combination Skin?
Which are Lbel Regression Jour Protective Complex With Spf 15 Facial Day Normal To Combination Skin 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 Regression Jour Protective Complex With Spf 15 Facial Day Normal To Combination Skin 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)
- SOY PROTEIN (UNII: R44IWB3RN5)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- PEA (UNII: W4X7H8GYFM)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MANNITOL (UNII: 3OWL53L36A)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- C20-22 ALKYL PHOSPHATE (UNII: L4VKP0Y7RP)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- 2-HYDROXYETHYL ACRYLATE (UNII: 25GT92NY0C)
- C20-22 ALCOHOLS (UNII: O4M0347C6A)
- TROLAMINE (UNII: 9O3K93S3TK)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) (UNII: 59TL3WG5CO)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SORBIC ACID (UNII: X045WJ989B)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
- YEAST (UNII: 3NY3SM6B8U)
- ETHYLPARABEN (UNII: 14255EXE39)
- CHLORELLA VULGARIS (UNII: RYQ4R60M02)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3)
- D&C BLUE NO. 4 (UNII: 0KSY80VYS3)
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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".