NDC 72934-2111 Hydrocortisone 2.5% / Iodoquinol 1% / Ketoconazole 2%
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72934 - Sincerus Florida, Llc
- 72934-2111 - Hydrocortisone 2.5% / Iodoquinol 1% / Ketoconazole 2%
Product Characteristics
Product Packages
NDC Code 72934-2111-2
Package Description: 30 g in 1 BOTTLE, PUMP
Product Details
What is NDC 72934-2111?
Which are Hydrocortisone 2.5% / Iodoquinol 1% / Ketoconazole 2% UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCORTISONE (UNII: WI4X0X7BPJ)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
- IODOQUINOL (UNII: 63W7IE88K8)
- IODOQUINOL (UNII: 63W7IE88K8) (Active Moiety)
- KETOCONAZOLE (UNII: R9400W927I)
- KETOCONAZOLE (UNII: R9400W927I) (Active Moiety)
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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".