NDC 76348-590 Hemporrhoid
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76348-590?
What are the uses for Hemporrhoid?
Which are Hemporrhoid UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Hemporrhoid 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:
- CARYOPHYLLENE (UNII: BHW853AU9H)
- .BETA.-PINENE (UNII: 4MS8VHZ1HJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- WHITE WAX (UNII: 7G1J5DA97F)
- HUMULENE (UNII: 54W56MD2WD)
- MYRCENE (UNII: 3M39CZS25B)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- EUCALYPTOL (UNII: RV6J6604TK)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- .ALPHA.-PINENE (UNII: JPF3YI7O34)
- NEROLIDOL (UNII: QR6IP857S6)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- TOCOPHEROL (UNII: R0ZB2556P8)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- JOJOBA OIL (UNII: 724GKU717M)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
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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".