NDC 59434-001 Ala-septic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59434 - Ala-septic Pharmaceutical Research Llc
- 59434-001 - Ala-septic
Product Packages
NDC Code 59434-001-04
Package Description: 100 g in 1 PACKAGE
Product Details
What is NDC 59434-001?
What are the uses for Ala-septic?
Which are Ala-septic UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Ala-septic 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 VERA WHOLE (UNII: KIZ4X2EHYX)
- WATER (UNII: 059QF0KO0R)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- LICORICE (UNII: 61ZBX54883)
- IODOQUINOL (UNII: 63W7IE88K8)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- LARREA TRIDENTATA WHOLE (UNII: B755J144H1)
- LAURETH-7 (UNII: Z95S6G8201)
- TEA TREE OIL (UNII: VIF565UC2G)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ALCOHOL (UNII: 3K9958V90M)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Ala-septic?
- RxCUI: 317152 - salicylic acid 2 % Topical Cream
- RxCUI: 317152 - salicylic acid 20 MG/ML Topical Cream
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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".