NDC 58559-001 Relief Pain Relieving Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 58559-001?
What are the uses for Relief Pain Relieving Cream?
Which are Relief Pain Relieving Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Relief Pain Relieving 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:
- ALOE (UNII: V5VD430YW9)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ORANGE OIL (UNII: AKN3KSD11B)
- PALMAROSA OIL (UNII: 0J3G3O53ST)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- WATER (UNII: 059QF0KO0R)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GLYCERIN (UNII: PDC6A3C0OX)
- ARGININE (UNII: 94ZLA3W45F)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- TOCOPHEROL (UNII: R0ZB2556P8)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Relief Pain Relieving Cream?
- RxCUI: 1291226 - menthol 2.5 % Topical Cream
- RxCUI: 1291226 - menthol 25 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".