NDC 58039-322 Saniclean Alcohol Antiseptic 70% Topical Solution Gel, Lemon Scented (hp2513)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58039 - Hppe, Llc
- 58039-322 - Saniclean Alcohol Antiseptic 70% Topical Solution Gel, Lemon Scented (hp2513)
Product Packages
NDC Code 58039-322-01
Package Description: 1000000 mL in 1 CONTAINER
Product Details
What is NDC 58039-322?
What are the uses for Saniclean Alcohol Antiseptic 70% Topical Solution Gel, Lemon Scented (hp2513)?
Which are Saniclean Alcohol Antiseptic 70% Topical Solution Gel, Lemon Scented (hp2513) UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Saniclean Alcohol Antiseptic 70% Topical Solution Gel, Lemon Scented (hp2513) 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)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- WATER (UNII: 059QF0KO0R)
- ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
What is the NDC to RxNorm Crosswalk for Saniclean Alcohol Antiseptic 70% Topical Solution Gel, Lemon Scented (hp2513)?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
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[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".