NDC 71414-305 Dehydrated Alcohol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71414 - Flon Laboratories Llc
- 71414-305 - Dehydrated Alcohol
Product Packages
NDC Code 71414-305-05
Package Description: 5 VIAL in 1 CARTON / 5 mL in 1 VIAL
Product Details
What is NDC 71414-305?
What are the uses for Dehydrated Alcohol?
Which are Dehydrated Alcohol UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Dehydrated Alcohol?
- RxCUI: 1869281 - ethanol 98 % in 5 ML Injection
- RxCUI: 1869281 - 5 ML ethanol 0.98 ML/ML Injection
- RxCUI: 1869281 - ethanol 98 % per 5 ML Injection
* 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".