NDC 61589-1905 No7 Soft And Sheer Tinted Moisturiser Medium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61589 - Bcm Cosmetique Sas
- 61589-1905 - No7 Soft And Sheer Tinted Moisturiser Medium
Product Packages
NDC Code 61589-1905-7
Package Description: 1 TUBE in 1 CARTON / 50 mL in 1 TUBE
Product Details
What is NDC 61589-1905?
What are the uses for No7 Soft And Sheer Tinted Moisturiser Medium?
Which are No7 Soft And Sheer Tinted Moisturiser Medium UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are No7 Soft And Sheer Tinted Moisturiser Medium 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PETROLATUM (UNII: 4T6H12BN9U)
- MINERAL OIL (UNII: T5L8T28FGP)
- POLYOXYL 100 STEARATE (UNII: YD01N1999R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- TALC (UNII: 7SEV7J4R1U)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- EDETATE SODIUM (UNII: MP1J8420LU)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".