NDC 80441-001 Sirenol Antiseptic Topical
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 80441-001-01
Package Description: 6 NOT APPLICABLE in 1 PACKAGE / 5 mL in 1 NOT APPLICABLE
NDC Code 80441-001-02
Package Description: 10 NOT APPLICABLE in 1 PACKAGE / 5 mL in 1 NOT APPLICABLE
NDC Code 80441-001-03
Package Description: 20 NOT APPLICABLE in 1 PACKAGE / 5 mL in 1 NOT APPLICABLE
NDC Code 80441-001-04
Package Description: 100 NOT APPLICABLE in 1 PACKAGE / 5 mL in 1 NOT APPLICABLE
NDC Code 80441-001-05
Package Description: 1000 NOT APPLICABLE in 1 PACKAGE / 5 mL in 1 NOT APPLICABLE
NDC Code 80441-001-06
Package Description: 60 NOT APPLICABLE in 1 BOTTLE / 150 mL in 1 NOT APPLICABLE
NDC Code 80441-001-07
Package Description: 80 NOT APPLICABLE in 1 BOTTLE / 200 mL in 1 NOT APPLICABLE
NDC Code 80441-001-08
Package Description: 100 NOT APPLICABLE in 1 BOTTLE / 250 mL in 1 NOT APPLICABLE
NDC Code 80441-001-09
Package Description: 25 mL in 1 BOTTLE
NDC Code 80441-001-10
Package Description: 50 mL in 1 BOTTLE
NDC Code 80441-001-11
Package Description: 100 mL in 1 BOTTLE
NDC Code 80441-001-12
Package Description: 150 mL in 1 BOTTLE
NDC Code 80441-001-13
Package Description: 200 mL in 1 BOTTLE
NDC Code 80441-001-14
Package Description: 250 mL in 1 BOTTLE
NDC Code 80441-001-15
Package Description: 500 mL in 1 BOTTLE
NDC Code 80441-001-16
Package Description: 1000 mL in 1 BOTTLE
NDC Code 80441-001-17
Package Description: 3785 mL in 1 BOTTLE
NDC Code 80441-001-18
Package Description: 5000 mL in 1 BOTTLE
NDC Code 80441-001-19
Package Description: 10000 mL in 1 BOTTLE
Product Details
What is NDC 80441-001?
What are the uses for Sirenol Antiseptic Topical?
Which are Sirenol Antiseptic Topical UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Sirenol Antiseptic Topical 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Sirenol Antiseptic Topical?
- RxCUI: 1039339 - ethanol 80 % Topical Solution
- RxCUI: 1039339 - ethanol 0.8 ML/ML Topical Solution
* 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".