NDC 65923-616 Sound Body Extra Strength Cold And Hot
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65923 - United Exchange Corp.
- 65923-616 - Sound Body Extra Strength Cold And Hot
Product Packages
NDC Code 65923-616-35
Package Description: 1 TUBE in 1 CARTON / 35.4 g in 1 TUBE
Product Details
What is NDC 65923-616?
What are the uses for Sound Body Extra Strength Cold And Hot?
Which are Sound Body Extra Strength Cold And Hot UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Sound Body Extra Strength Cold And Hot 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:
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- LANOLIN (UNII: 7EV65EAW6H)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Sound Body Extra Strength Cold And Hot?
- RxCUI: 311500 - menthol 10 % / methyl salicylate 30 % Topical Cream
- RxCUI: 311500 - menthol 100 MG/ML / methyl salicylate 300 MG/ML Topical Cream
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[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".