NDC 68071-2473 Silver Sulfadiazine
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68071-2473?
What are the uses for Silver Sulfadiazine?
Which are Silver Sulfadiazine UNII Codes?
The UNII codes for the active ingredients in this product are:
- SILVER SULFADIAZINE (UNII: W46JY43EJR)
- SULFADIAZINE (UNII: 0N7609K889) (Active Moiety)
Which are Silver Sulfadiazine 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:
- WATER (UNII: 059QF0KO0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PETROLATUM (UNII: 4T6H12BN9U)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- METHYLPARABEN (UNII: A2I8C7HI9T)
What is the NDC to RxNorm Crosswalk for Silver Sulfadiazine?
- RxCUI: 106351 - silver sulfADIAZINE 1 % Topical Cream
- RxCUI: 106351 - silver sulfadiazine 10 MG/ML Topical Cream
- RxCUI: 106351 - silver sulfadiazine 1 % Topical Cream
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Patient Education
Silver Sulfadiazine
Silver sulfadiazine, a sulfa drug, is used to prevent and treat infections of second- and third-degree burns. It kills a wide variety of bacteria. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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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".