NDC 73347-117 Rapid-ease Pain Relief Topical Analgesic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73347 - Rapid-ease
- 73347-117 - Rapid-ease Pain Relief
Product Characteristics
Product Packages
NDC Code 73347-117-01
Package Description: 1 TUBE in 1 CARTON / 120 g in 1 TUBE
NDC Code 73347-117-02
Package Description: 1 TUBE in 1 CARTON / 60 g in 1 TUBE
Product Details
What is NDC 73347-117?
What are the uses for Rapid-ease Pain Relief Topical Analgesic?
Which are Rapid-ease Pain Relief Topical Analgesic 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 Rapid-ease Pain Relief Topical Analgesic 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:
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- GLYCERIN (UNII: PDC6A3C0OX)
- MACADAMIA OIL (UNII: 515610SU8C)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- COMFREY LEAF (UNII: DG4F8T839X)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Rapid-ease Pain Relief Topical Analgesic?
- 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".