NDC 68788-9818 Thermazene
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68788 - Preferred Pharmaceuticals, Inc
- 68788-9818 - Thermazene
Product Packages
NDC Code 68788-9818-2
Package Description: 20 g in 1 TUBE
NDC Code 68788-9818-5
Package Description: 50 g in 1 TUBE
Product Details
What is NDC 68788-9818?
What are the uses for Thermazene?
Which are Thermazene UNII Codes?
The UNII codes for the active ingredients in this product are:
- SILVER SULFADIAZINE (UNII: W46JY43EJR)
- SILVER SULFADIAZINE (UNII: W46JY43EJR) (Active Moiety)
Which are Thermazene 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)
- 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 Thermazene?
- RxCUI: 106351 - silver sulfADIAZINE 1 % Topical Cream
- RxCUI: 106351 - silver sulfadiazine 10 MG/ML Topical Cream
- RxCUI: 106351 - silver sulfadiazine 1 % Topical Cream
- RxCUI: 208187 - Thermazene 1 % Topical Cream
- RxCUI: 208187 - silver sulfadiazine 10 MG/ML Topical Cream [Thermazene]
* 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".