NDC 52512-130 Dr. Numb
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 52512-130?
What are the uses for Dr. Numb?
Which are Dr. Numb UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Dr. Numb 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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- CARBOMER HOMOPOLYMER TYPE B (UNII: HHT01ZNK31)
What is the NDC to RxNorm Crosswalk for Dr. Numb?
- RxCUI: 1366789 - lidocaine 5 % Rectal Cream
- RxCUI: 1366789 - lidocaine 50 MG/ML Rectal Cream
- RxCUI: 1366794 - Dr. Numb 5 % Rectal Cream
- RxCUI: 1366794 - lidocaine 50 MG/ML Rectal Cream [Dr. Numb]
- RxCUI: 1366794 - Dr. Numb 50 MG/ML 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".