NDC 61722-239 Flormar Delicious Lip Stylo Sunscreen Broad Spectrum Spf 15 Ds14 Rise Of Modern City
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 61722-239?
What are the uses for Flormar Delicious Lip Stylo Sunscreen Broad Spectrum Spf 15 Ds14 Rise Of Modern City?
Which are Flormar Delicious Lip Stylo Sunscreen Broad Spectrum Spf 15 Ds14 Rise Of Modern City UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Flormar Delicious Lip Stylo Sunscreen Broad Spectrum Spf 15 Ds14 Rise Of Modern City 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:
- DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
- TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MICA (UNII: V8A1AW0880)
- TRIISOSTEARYL CITRATE (UNII: 50XT325OOH)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- LAUROYL LYSINE (UNII: 113171Q70B)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- D&C RED NO. 34 (UNII: BAN556989E)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
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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".