NDC 0395-0119 Ivy Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0395 - Humco Holding Group, Inc.
- 0395-0119 - Ivy Wash
Product Packages
NDC Code 0395-0119-96
Package Description: 117 mL in 1 BOTTLE
Product Details
What is NDC 0395-0119?
What are the uses for Ivy Wash?
Which are Ivy Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
Which are Ivy Wash 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)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- NONOXYNOL-9 (UNII: 48Q180SH9T)
What is the NDC to RxNorm Crosswalk for Ivy Wash?
- RxCUI: 1247251 - pramoxine HCl 1 % Medicated Liquid Soap
- RxCUI: 1247251 - pramoxine hydrochloride 10 MG/ML Medicated Liquid Soap
- RxCUI: 1247251 - pramoxine hydrochloride 1 % Medicated Liquid Soap
* 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".