NDC 58133-075 Red Lion Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58133 - Cosmetic Specialty Labs, Inc.
- 58133-075 - Red Lion Relief
Product Packages
NDC Code 58133-075-04
Package Description: 115 g in 1 TUBE
Product Details
What is NDC 58133-075?
Which are Red Lion Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Red Lion Relief 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 LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- 1,3-BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ORANGE OIL (UNII: AKN3KSD11B)
- PALMAROSA OIL (UNII: 0J3G3O53ST)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- MENTHA PIPERITA LEAF (UNII: A389O33LX6)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATER (UNII: 059QF0KO0R)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- SORBITOL (UNII: 506T60A25R)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Red Lion Relief?
- RxCUI: 1442261 - menthol 3 % Topical Cream
- RxCUI: 1442261 - menthol 30 MG/ML Topical Cream
- RxCUI: 1487428 - Red Lion Relief 30 MG/ML Topical Cream
- RxCUI: 1487428 - menthol 30 MG/ML Topical Cream [Red Lion Relief]
* Please review the disclaimer below.
[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".