NDC 64539-014 Folrex Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 64539-014?
What are the uses for Folrex Cream?
Which are Folrex Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Folrex Cream 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:
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- CETETH-20 (UNII: I835H2IHHX)
- STEARETH-20 (UNII: L0Q8IK9E08)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- BISULFITE ION (UNII: OJ9787WBLU)
- FOLIC ACID (UNII: 935E97BOY8)
- COUMARIN (UNII: A4VZ22K1WT)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- LINALOOL, (-)- (UNII: 3U21E3V8I2)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GERANIOL (UNII: L837108USY)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
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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".