NDC 72284-0002 Im Clear Cica Sunstick
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 72284-0002?
Which are Im Clear Cica Sunstick UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Im Clear Cica Sunstick 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:
- DIBUTYL LAUROYL GLUTAMIDE (UNII: 3V7K3IA58X)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- XYLITOL (UNII: VCQ006KQ1E)
- LIMONIA ACIDISSIMA WOOD (UNII: 04X926XD7Z)
- BAMBUSA VULGARIS LEAF (UNII: EMY54R518C)
- LAVANDULA ANGUSTIFOLIA WHOLE (UNII: 51217XIL5L)
- MATRICARIA CHAMOMILLA FLOWERING TOP (UNII: 3VNC7T6Z02)
- LONICERA CAPRIFOLIUM WHOLE (UNII: 4F67A99YTF)
- ORIGANUM VULGARE SUBSP. HIRTUM WHOLE (UNII: 38SNL0F81Z)
- THYMUS VULGARIS WHOLE (UNII: 8L72OKJ7II)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)
- CYMBOPOGON SCHOENANTHUS OIL (UNII: XE7K568ILO)
- ADENOSINE (UNII: K72T3FS567)
- XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
- ISODODECANE (UNII: A8289P68Y2)
- DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
- DIBUTYL ETHYLHEXANOYL GLUTAMIDE (UNII: 0IAF2L30VS)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- LEVOMENOL (UNII: 24WE03BX2T)
- ANHYDROXYLITOL (UNII: 8XWR7NN42F)
- OLDENLANDIA DIFFUSA (UNII: 291PPU5K9I)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
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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".