NDC 61582-533 Everflex Topical Analgesic Pain Relief With Msm
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61582 - Natures Sunshine Products, Inc.
- 61582-533 - Everflex Topical Analgesic Pain Relief With Msm
Product Packages
NDC Code 61582-533-01
Package Description: 58.7 mL in 1 JAR
Product Details
What is NDC 61582-533?
What are the uses for Everflex Topical Analgesic Pain Relief With Msm?
Which are Everflex Topical Analgesic Pain Relief With Msm UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Everflex Topical Analgesic Pain Relief With Msm 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:
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL MYRISTOLEATE (UNII: 87P8K33Q5X)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- CETYL MYRISTATE (UNII: 7OPL833Q4D)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- CETYL PALMITOLEATE (UNII: 962I97113K)
- CETYL OLEATE (UNII: 78K2L26L8N)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
What is the NDC to RxNorm Crosswalk for Everflex Topical Analgesic Pain Relief With Msm?
- RxCUI: 416982 - menthol 1.25 % Topical Cream
- RxCUI: 416982 - menthol 12.5 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".