NDC 51068-507 Activon Ultra Strength Arthritis
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51068 - Family First Pharmaceuticals, Inc.
- 51068-507 - Activon Ultra Strength Arthritis
Product Packages
NDC Code 51068-507-01
Package Description: 1 CANISTER in 1 CARTON / 57 g in 1 CANISTER
Product Details
What is NDC 51068-507?
What are the uses for Activon Ultra Strength Arthritis?
Which are Activon Ultra Strength Arthritis UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
Which are Activon Ultra Strength Arthritis 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)
- ALCOHOL (UNII: 3K9958V90M)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM STEARATE (UNII: QU7E2XA9TG)
- STEARETH-21 (UNII: 53J3F32P58)
- EDETATE SODIUM (UNII: MP1J8420LU)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Activon Ultra Strength Arthritis?
- RxCUI: 1148638 - menthol 5.14 % Topical Cream
- RxCUI: 1148638 - menthol 51.4 MG/ML Topical Cream
- RxCUI: 1148640 - ActivOn Ultra Strength Joint & Muscle 5.138 % Topical Cream
- RxCUI: 1148640 - menthol 51.4 MG/ML Topical Cream [ActivOn Joint & Muscle]
- RxCUI: 1148640 - ActivOn Joint & Muscle 51.4 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".