NDC 50967-357 Procort
1.85% Hydrocortisone Acetate - 1.15% Pramoxine Hci Cream Cream Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50967 - Womens Choice Pharmaceuticals Llc
- 50967-357 - Procort
Product Characteristics
Product Packages
NDC Code 50967-357-60
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON / 1 TUBE, WITH APPLICATOR in 1 TUBE, WITH APPLICATOR / 60 g in 1 TUBE, WITH APPLICATOR
Product Details
What is NDC 50967-357?
What are the uses for Procort?
What are Procort Active Ingredients?
Which are Procort UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCORTISONE ACETATE (UNII: 3X7931PO74)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
Which are Procort 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:
- AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
- BUTYL ESTER OF METHYL VINYL ETHER-MALEIC ANHYDRIDE COPOLYMER (125 KD) (UNII: 389H2R62BD)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLOXAMER 124 (UNII: 1S66E28KXA)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- WATER (UNII: 059QF0KO0R)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
What is the NDC to RxNorm Crosswalk for Procort?
- RxCUI: 1114854 - hydrocortisone acetate 1.85 % / pramoxine HCl 1.15 % Rectal Cream
- RxCUI: 1114854 - hydrocortisone acetate 18.5 MG/ML / pramoxine hydrochloride 11.5 MG/ML Rectal Cream
- RxCUI: 1115730 - ProCort 1.85 % / 1.15 % Rectal Cream
- RxCUI: 1115730 - hydrocortisone acetate 18.5 MG/ML / pramoxine hydrochloride 11.5 MG/ML Rectal Cream [Procort 1.85/1.15]
- RxCUI: 1115730 - Procort 1.85 % / 1.15 % (hydrocortisone acetate / pramoxine HCl) Rectal Cream
Which are the Pharmacologic Classes for Procort?
* Please review the disclaimer below.
Patient Education
Hydrocortisone Rectal
Rectal hydrocortisone is used along with other medications to treat proctitis (swelling in the rectum) and ulcerative colitis (a condition which causes swelling and sores in the lining of the large intestine and rectum). It is also used to relieve itching and swelling from hemorrhoids and other rectal problems. Hydrocortisone is in a class of medications called corticosteroids. It works by activating natural substances in the skin to reduce swelling, redness, and itching.
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Pramoxine
Pramoxine is used to temporarily relieve pain and itching from insect bites; poison ivy, poison oak, or poison sumac; minor cuts, scrapes, or burns; minor skin irritation or rashes; or dry, itchy skin. Pramoxine also may be used to treat soreness, burning, itching, and pain from hemorrhoids (''piles'') and other minor rectal irritations or itching. Pramoxine is in a class of medications called topical anesthetics. It works by stopping nerves from sending pain signals.
[Learn More]
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".