NDC 29500-2438 Anesthetic Hemorrhoidal With Aloe
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What is NDC 29500-2438?
What are the uses for Anesthetic Hemorrhoidal With Aloe?
Which are Anesthetic Hemorrhoidal With Aloe UNII Codes?
The UNII codes for the active ingredients in this product are:
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Anesthetic Hemorrhoidal With Aloe 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:
- BALSAM PERU (UNII: 8P5F881OCY)
- BENZYL BENZOATE (UNII: N863NB338G)
- CALCIUM PHOSPHATE (UNII: 97Z1WI3NDX)
- COCOA BUTTER (UNII: 512OYT1CRR)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- KAOLIN (UNII: 24H4NWX5CO)
- MINERAL OIL (UNII: T5L8T28FGP)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
What is the NDC to RxNorm Crosswalk for Anesthetic Hemorrhoidal With Aloe?
- RxCUI: 1294330 - pramoxine HCl 1 % / zinc oxide 12.5 % Topical Ointment
- RxCUI: 1294330 - pramoxine hydrochloride 0.01 MG/MG / zinc oxide 0.125 MG/MG Topical Ointment
- RxCUI: 1294330 - Pramoxine hydrochloride 0.01 MG/MG / ZNO 0.125 MG/MG Topical Ointment
- RxCUI: 1294330 - pramoxine hydrochloride 1 % / zinc oxide 12.5 % Topical Ointment
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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".