NDC 79753-012 Liplux Spf 30 Lip Balm
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79753 - Coola Llc
- 79753-012 - Liplux
Product Packages
NDC Code 79753-012-01
Package Description: 4.2 g in 1 TUBE
Product Details
What is NDC 79753-012?
What are the uses for Liplux Spf 30 Lip Balm?
Which are Liplux Spf 30 Lip Balm UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Liplux Spf 30 Lip Balm 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:
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- ASTROCARYUM VULGARE KERNEL OIL (UNII: 1IQY04O559)
- COCONUT OIL (UNII: Q9L0O73W7L)
- BEHENYL BEHENATE (UNII: K8NU647RJ0)
- POLYHYDROXYSTEARIC ACID STEARATE (UNII: 8KQ7I65XZE)
- CANDELILLA WAX (UNII: WL0328HX19)
- THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- TOCOPHEROL (UNII: R0ZB2556P8)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- REBAUDIOSIDE A (UNII: B3FUD0528F)
- JOJOBA OIL (UNII: 724GKU717M)
- CASTOR OIL (UNII: D5340Y2I9G)
- ROSEMARY (UNII: IJ67X351P9)
- ROSA CANINA FRUIT (UNII: 3TNW8D08V3)
- LEVOMENOL (UNII: 24WE03BX2T)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- RASPBERRY SEED OIL (UNII: 9S8867952A)
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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".