NDC 70359-4106 Poxiezzz
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 70359-4106?
What are the uses for Poxiezzz?
Which are Poxiezzz UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Poxiezzz 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)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
- COCO-GLYCERIDES (UNII: ISE9I7DNUG)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- OLEIC ACID (UNII: 2UMI9U37CP)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
What is the NDC to RxNorm Crosswalk for Poxiezzz?
- RxCUI: 1733853 - menthol 1 % / zinc oxide 4 % Topical Spray
- RxCUI: 1733853 - menthol 10 MG/ML / zinc oxide 40 MG/ML Topical Spray
- RxCUI: 1733853 - Menthol 10 MG/ML / ZNO 40 MG/ML Topical Spray
* 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".