NDC 58484-100 Mr Dudleys Topical Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58484 - Dudley Wellness Company Inc
- 58484-100 - Mr Dudleys Topical Pain Relief
Product Packages
NDC Code 58484-100-01
Package Description: .2 g in 1 BOTTLE
NDC Code 58484-100-05
Package Description: 1.4 g in 1 BOTTLE
NDC Code 58484-100-20
Package Description: 57 g in 1 BOTTLE
NDC Code 58484-100-45
Package Description: 128 g in 1 BOTTLE
Product Details
What is NDC 58484-100?
What are the uses for Mr Dudleys Topical Pain Relief?
Which are Mr Dudleys Topical Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Mr Dudleys Topical Pain 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ACRYLAMIDE (UNII: 20R035KLCI)
- EUGENOL (UNII: 3T8H1794QW)
- METHYL EUGENOL (UNII: 29T9VA6R7M)
- NUTMEG OIL (UNII: Z1CLM48948)
- METHYL ISOEUGENOL (UNII: 46RN7Q97DE)
- 4-ALLYL-2,6-DIMETHOXYPHENOL (UNII: 8VF00YWP89)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Mr Dudleys Topical Pain Relief?
- RxCUI: 1291226 - menthol 2.5 % Topical Cream
- RxCUI: 1291226 - menthol 25 MG/ML Topical Cream
* 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".