NDC 75001-204 Devolver Premium Tissue
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 75001-204-01
Package Description: 100 g in 1 POUCH
NDC Code 75001-204-02
Package Description: 100 g in 1 POUCH
NDC Code 75001-204-03
Package Description: 100 g in 1 POUCH
NDC Code 75001-204-04
Package Description: 100 g in 1 POUCH
NDC Code 75001-204-05
Package Description: 335 g in 1 POUCH
NDC Code 75001-204-06
Package Description: 335 g in 1 POUCH
NDC Code 75001-204-07
Package Description: 100 g in 1 POUCH
NDC Code 75001-204-08
Package Description: 300 g in 1 BOTTLE
NDC Code 75001-204-09
Package Description: 400 g in 1 BOTTLE
NDC Code 75001-204-10
Package Description: 500 g in 1 BOTTLE
NDC Code 75001-204-11
Package Description: 800 g in 1 BOTTLE
NDC Code 75001-204-12
Package Description: 1100 g in 1 BOTTLE
Product Details
What is NDC 75001-204?
What are the uses for Devolver Premium Tissue?
Which are Devolver Premium Tissue UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Devolver Premium Tissue 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:
- ALOE FEROX LEAF (UNII: 0D145J8EME)
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- LIME (CALCIUM OXIDE) (UNII: C7X2M0VVNH)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
What is the NDC to RxNorm Crosswalk for Devolver Premium Tissue?
- RxCUI: 1307051 - ethanol 75 % Medicated Pad
- RxCUI: 1307051 - ethanol 0.75 ML/ML Medicated Pad
- RxCUI: 1307051 - ethanol 75 % Hand Sanitizer Wipes
* 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".