NDC 61601-0082 Lipstick Queen Endless Summer Broad Spectrum Spf 15 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61601 - Space Brands Limited
- 61601-0082 - Lipstick Queen Endless Summer Broad Spectrum Spf 15 Sunscreen
Product Characteristics
BROWN (C48332 - HANG TEN)
Product Packages
NDC Code 61601-0082-3
Package Description: 1 APPLICATOR in 1 CARTON / 3.5 g in 1 APPLICATOR
Product Details
What is NDC 61601-0082?
What are the uses for Lipstick Queen Endless Summer Broad Spectrum Spf 15 Sunscreen?
Which are Lipstick Queen Endless Summer Broad Spectrum Spf 15 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Lipstick Queen Endless Summer Broad Spectrum Spf 15 Sunscreen 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:
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- CASTOR OIL (UNII: D5340Y2I9G)
- CORN OIL (UNII: 8470G57WFM)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
- ISOSTEARYL HYDROXYSTEARATE (UNII: F7540880P0)
- CANDELILLA WAX (UNII: WL0328HX19)
- TRIISOSTEARYL CITRATE (UNII: 50XT325OOH)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
- TRIMETHYLOLPROPANE TRIISOSTEARATE (UNII: Y32A6D7C6L)
- TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TOCOPHEROL (UNII: R0ZB2556P8)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
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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".