NDC 62742-4063 No Foundation Foundation No.1 Fair To Light
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 62742-4063?
What are the uses for No Foundation Foundation No.1 Fair To Light?
Which are No Foundation Foundation No.1 Fair To Light UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are No Foundation Foundation No.1 Fair To Light 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- MICA (UNII: V8A1AW0880)
- DEANOL (UNII: 2N6K9DRA24)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- .ALPHA.-TOCOPHEROL LINOLEATE, D- (UNII: G0N132Q0ED)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CERAMIDE 2 (UNII: C04977SRJ5)
- DATE (UNII: H3O7QI5HY7)
- PEG-10 RAPESEED STEROL (UNII: 258O76T85M)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- LAURETH-7 (UNII: Z95S6G8201)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
* 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".