NDC 10956-799 Reeses Pinworm Itch Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10956 - Reese Pharmaceutical Co
- 10956-799 - Reeses
Product Packages
NDC Code 10956-799-20
Package Description: 89 g in 1 PACKAGE
Product Details
What is NDC 10956-799?
What are the uses for Reeses Pinworm Itch Relief?
Which are Reeses Pinworm Itch Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
Which are Reeses Pinworm Itch Relief 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
What is the NDC to RxNorm Crosswalk for Reeses Pinworm Itch Relief?
- RxCUI: 1039541 - pramoxine HCl 1 % Medicated Pad
- RxCUI: 1039541 - pramoxine hydrochloride 10 MG/ML Medicated Pad
- RxCUI: 1039541 - pramoxine hydrochloride 1 % Medicated Pad
- RxCUI: 1039541 - pramoxine hydrochloride 1 % Medicated Wipe
* Please review the disclaimer below.
Patient Education
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.
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* 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".