NDC 41190-210 Advanced Antiseptic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41190 - Wakefern Food Corporation
- 41190-210 - Advanced Antiseptic
Product Packages
NDC Code 41190-210-12
Package Description: 1.5 L in 1 BOTTLE, PLASTIC
NDC Code 41190-210-86
Package Description: 1 L in 1 BOTTLE, PLASTIC
Product Details
What is NDC 41190-210?
What are the uses for Advanced Antiseptic?
Which are Advanced Antiseptic UNII Codes?
The UNII codes for the active ingredients in this product are:
- EUCALYPTOL (UNII: RV6J6604TK)
- EUCALYPTOL (UNII: RV6J6604TK) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- METHYL SALICYLATE (UNII: LAV5U5022Y) (Active Moiety)
- THYMOL (UNII: 3J50XA376E)
- THYMOL (UNII: 3J50XA376E) (Active Moiety)
Which are Advanced Antiseptic 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- SORBITOL (UNII: 506T60A25R)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
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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".