NDC 50414-100 Hand Gel Prolim Instant Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50414 - Prolim Quimica Avancada Ltda.
- 50414-100 - Hand Gel Prolim Instant Hand Sanitizer
Product Packages
NDC Code 50414-100-01
Package Description: 60 mL in 1 BOTTLE, PLASTIC
NDC Code 50414-100-02
Package Description: 80 mL in 1 BOTTLE, PLASTIC
NDC Code 50414-100-03
Package Description: 100 mL in 1 BOTTLE, PLASTIC
NDC Code 50414-100-04
Package Description: 200 mL in 1 BOTTLE, PUMP
NDC Code 50414-100-05
Package Description: 500 mL in 1 BOTTLE, PUMP
NDC Code 50414-100-06
Package Description: 1000 mL in 1 BOTTLE, PUMP
NDC Code 50414-100-07
Package Description: 5000 mL in 1 BOTTLE, PLASTIC
NDC Code 50414-100-08
Package Description: 1 BAG in 1 BOX / 800 mL in 1 BAG
NDC Code 50414-100-09
Package Description: 1 BAG in 1 BOX / 1200 mL in 1 BAG
Product Details
What is NDC 50414-100?
What are the uses for Hand Gel Prolim Instant Hand Sanitizer?
Which are Hand Gel Prolim Instant Hand Sanitizer 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 Hand Gel Prolim Instant Hand Sanitizer?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
* 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".