NDC 54162-229 Caladrox
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54162 - Geritrex Llc
- 54162-229 - Caladrox
Product Packages
NDC Code 54162-229-04
Package Description: 113 g in 1 TUBE
Product Details
What is NDC 54162-229?
What are the uses for Caladrox?
Which are Caladrox UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Caladrox 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- LANOLIN (UNII: 7EV65EAW6H)
- PHENOL (UNII: 339NCG44TV)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- THYMOL (UNII: 3J50XA376E)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Caladrox?
- RxCUI: 744868 - menthol 0.44 % / zinc oxide 20 % Topical Ointment
- RxCUI: 744868 - menthol 0.0044 MG/MG / zinc oxide 0.2 MG/MG Topical Ointment
- RxCUI: 744868 - Menthol 0.0044 MG/MG / ZNO 0.2 MG/MG Topical Ointment
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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".