NDC 68040-702 Alcortin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68040 - Primus Pharmaceuticals
- 68040-702 - Alcortin
Product Packages
NDC Code 68040-702-08
Package Description: 64 CARTON in 1 BOX / 10 PACKET in 1 CARTON / 2 g in 1 PACKET (68040-702-02)
NDC Code 68040-702-13
Package Description: 12 CARTON in 1 BOX / 24 PACKET in 1 CARTON / 2 g in 1 PACKET
Product Details
What is NDC 68040-702?
Which are Alcortin 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)
What is the NDC to RxNorm Crosswalk for Alcortin?
- RxCUI: 1191414 - Alcortin 1 % / 2 % Topical Gel
- RxCUI: 1191414 - hydrocortisone 0.02 MG/MG / iodoquinol 0.01 MG/MG Topical Gel [Alcortin]
- RxCUI: 1191414 - Alcortin (hydrocortisone 2 % / iodoquinol 1 % ) Topical Gel
- RxCUI: 544118 - iodoquinol 1 % / hydrocortisone 2 % Topical Gel
- RxCUI: 544118 - hydrocortisone 0.02 MG/MG / iodoquinol 0.01 MG/MG Topical Gel
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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".