NDC 60608-011 Bio-scriptives Lidum
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 60608-011?
What are the uses for Bio-scriptives Lidum?
Which are Bio-scriptives Lidum UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Bio-scriptives Lidum 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- CAPRYLIC/CAPRIC MONO/DIGLYCERIDES (UNII: U72Q2I8C85)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ARGININE HYDROCHLORIDE (UNII: F7LTH1E20Y)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ETHYL OLEATE (UNII: Z2Z439864Y)
- TOCOPHERSOLAN (UNII: O03S90U1F2)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TROLAMINE (UNII: 9O3K93S3TK)
- ALLANTOIN (UNII: 344S277G0Z)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- METHYL NICOTINATE (UNII: 7B1AVU9DJN)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
What is the NDC to RxNorm Crosswalk for Bio-scriptives Lidum?
- RxCUI: 1366789 - lidocaine 5 % Rectal Cream
- RxCUI: 1366789 - lidocaine 50 MG/ML Rectal Cream
- RxCUI: 1436083 - Bio-Scriptives Lidum 5 % Rectal Cream
- RxCUI: 1436083 - lidocaine 50 MG/ML Rectal Cream [Lidum]
- RxCUI: 1436083 - Lidum 5 % Rectal Cream
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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".