NDC 50125-001 Medessence Plus Homeopathic Nail
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50125 - Deep Cover Systems Llc
- 50125-001 - Medessence Plus
Product Packages
NDC Code 50125-001-10
Package Description: 10 mL in 1 PACKET
Product Details
What is NDC 50125-001?
What are the uses for Medessence Plus Homeopathic Nail?
Which are Medessence Plus Homeopathic Nail UNII Codes?
The UNII codes for the active ingredients in this product are:
- THUJA OCCIDENTALIS TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS TWIG (UNII: 1NT28V9397) (Active Moiety)
- ANTIMONY TRISULFIDE (UNII: F79059A38U)
- ANTIMONY (UNII: 9IT35J3UV3) (Active Moiety)
- DIOSCOREA VILLOSA EXTRACT (UNII: IWY3IWX2G8)
- DIOSCOREA VILLOSA EXTRACT (UNII: IWY3IWX2G8) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- BORIC ACID (UNII: R57ZHV85D4) (Active Moiety)
- CINNAMON (UNII: 5S29HWU6QB)
- CINNAMON (UNII: 5S29HWU6QB) (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".