NDC 82433-101 Hemorrhoidal-ointment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 82433-101?
What are the uses for Hemorrhoidal-ointment?
Which are Hemorrhoidal-ointment UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
Which are Hemorrhoidal-ointment 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 FIR LEAFY TWIG (UNII: H1TFV1454Z)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- LANOLIN (UNII: 7EV65EAW6H)
- LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- ALOE (UNII: V5VD430YW9)
- SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)
- GLYCERIN (UNII: PDC6A3C0OX)
- WITCH HAZEL (UNII: 101I4J0U34)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Hemorrhoidal-ointment?
- RxCUI: 2673304 - lidocaine 4 % / phenylephrine HCl 0.25 % Rectal Ointment
- RxCUI: 2673304 - lidocaine 0.04 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Ointment
* Please review the disclaimer below.
[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".