NDC 61722-233 Flormar Delicious Lip Stylo Sunscreen Broad Spectrum Spf 15 Ds06 Yeah It S Yellow
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 61722-233?
What are the uses for Flormar Delicious Lip Stylo Sunscreen Broad Spectrum Spf 15 Ds06 Yeah It S Yellow?
Which are Flormar Delicious Lip Stylo Sunscreen Broad Spectrum Spf 15 Ds06 Yeah It S Yellow 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 Ds06 Yeah It S Yellow 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)
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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".