NDC 51808-220 Sulfur Colloid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51808 - Anazaohealth Corporation
- 51808-220 - Sulfur Colloid
Product Packages
NDC Code 51808-220-01
Package Description: 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 KIT
Product Details
What is NDC 51808-220?
What are the uses for Sulfur Colloid?
Which are Sulfur Colloid UNII Codes?
The UNII codes for the active ingredients in this product are:
- GELATIN (UNII: 2G86QN327L)
- GELATIN (UNII: 2G86QN327L) (Active Moiety)
Which are Sulfur Colloid 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:
- SODIUM THIOSULFATE (UNII: HX1032V43M)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
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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".