NDC 76119-1441 Mally Face Defender Foundation Bb
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76119 - Mallygirl, Llc
- 76119-1441 - Mally Face Defender Foundation Bb
Product Packages
NDC Code 76119-1441-1
Package Description: 1 TUBE in 1 BOX / 53.2 mL in 1 TUBE
Product Details
What is NDC 76119-1441?
What are the uses for Mally Face Defender Foundation Bb?
Which are Mally Face Defender Foundation Bb UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Mally Face Defender Foundation Bb 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)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- PHYTANTRIOL (UNII: 8LVI07A72W)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- NYLON-12 (UNII: 446U8J075B)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- LYSINE (UNII: K3Z4F929H6)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
* Please review the disclaimer below.
[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".