NDC 69817-0201 Allopax
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69817 - Pharmagenetico Llc
- 69817-0201 - Allopax
Product Details
What is NDC 69817-0201?
Which are Allopax UNII Codes?
The UNII codes for the active ingredients in this product are:
- LORATADINE (UNII: 7AJO3BO7QN)
- LORATADINE (UNII: 7AJO3BO7QN) (Active Moiety)
- LEVOCETIRIZINE DIHYDROCHLORIDE (UNII: SOD6A38AGA)
- LEVOCETIRIZINE (UNII: 6U5EA9RT2O) (Active Moiety)
Which are Allopax 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:
- WATER (UNII: 059QF0KO0R)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- WHEAT GERM OIL (UNII: 14C97E680P)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
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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".