NDC 61924-214 Dermamed
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61924 - Dermarite Industries, Llc
- 61924-214 - Dermamed
Product Packages
NDC Code 61924-214-04
Package Description: 106 g in 1 TUBE
Product Details
What is NDC 61924-214?
What are the uses for Dermamed?
Which are Dermamed 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 Dermamed 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:
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- LANOLIN (UNII: 7EV65EAW6H)
- LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)
- PROPYLENE GLYCOL 1-(2-METHYLBUTYRATE) (UNII: 9Q5W5G6461)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- CORN OIL (UNII: 8470G57WFM)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PETROLATUM (UNII: 4T6H12BN9U)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- WATER (UNII: 059QF0KO0R)
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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".