NDC 54633-201 K2 Cold Therapy
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54633 - The Podiatree Co
- 54633-201 - K2 Cold Therapy
Product Packages
NDC Code 54633-201-13
Package Description: 88.72 mL in 1 BOTTLE
Product Details
What is NDC 54633-201?
What are the uses for K2 Cold Therapy?
Which are K2 Cold Therapy UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are K2 Cold Therapy 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M)
- ALCOHOL (UNII: 3K9958V90M)
- SIMMONDSIA CHINENSIS WHOLE (UNII: DFM16KFA82)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-20 (UNII: L0Q8IK9E08)
- UREA (UNII: 8W8T17847W)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for K2 Cold Therapy?
- RxCUI: 259249 - menthol 10 % Topical Gel
- RxCUI: 259249 - menthol 0.1 MG/MG Topical Gel
* 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".