NDC 54162-221 Dermadrox
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54162 - Geritrex Llc
- 54162-221 - Dermadrox
Product Packages
NDC Code 54162-221-01
Package Description: 113 g in 1 TUBE
NDC Code 54162-221-04
Package Description: 113 g in 1 JAR
Product Details
What is NDC 54162-221?
What are the uses for Dermadrox?
Which are Dermadrox UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (Active Moiety)
Which are Dermadrox 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:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- LANOLIN (UNII: 7EV65EAW6H)
- LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
- MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- VITAMIN A (UNII: 81G40H8B0T)
- VITAMIN D (UNII: 9VU1KI44GP)
- ZINC CHLORIDE (UNII: 86Q357L16B)
What is the NDC to RxNorm Crosswalk for Dermadrox?
- RxCUI: 1368022 - aluminum hydroxide 1.2 % Topical Ointment
- RxCUI: 1368022 - aluminum hydroxide 0.012 MG/MG Topical Ointment
* 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".