NDC 70186-595 Magic Foundation Flawless Long-lasting Coverage Sunscreen Broad Spectrum Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BROWN (C48332 - 2 FAIR)
BROWN (C48332 - 3 FAIR)
BROWN (C48332 - 3.5 FAIR)
BROWN (C48332 - 4 FAIR)
BROWN (C48332 - 4.5 MEDIUM)
BROWN (C48332 - 5 MEDIUM)
BROWN (C48332 - 6 MEDIUM)
BROWN (C48332 - 7 MEDIUM)
BROWN (C48332 - 8 MEDIUM)
Code Structure Chart
Product Details
What is NDC 70186-595?
What are the uses for Magic Foundation Flawless Long-lasting Coverage Sunscreen Broad Spectrum Spf 15?
Which are Magic Foundation Flawless Long-lasting Coverage Sunscreen Broad Spectrum Spf 15 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 Magic Foundation Flawless Long-lasting Coverage Sunscreen Broad Spectrum Spf 15 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)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- TALC (UNII: 7SEV7J4R1U)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- NYLON-12 (UNII: 446U8J075B)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- EDETATE SODIUM (UNII: MP1J8420LU)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
- FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)
* 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".