NDC 51393-4008 Scalp Dermatitis
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51393 - Forces Of Nature
- 51393-4008 - Scalp Dermatitis
Product Characteristics
Product Packages
NDC Code 51393-4008-1
Package Description: 11 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 51393-4008?
What are the uses for Scalp Dermatitis?
Which are Scalp Dermatitis UNII Codes?
The UNII codes for the active ingredients in this product are:
- URTICA DIOICA (UNII: 710FLW4U46)
- URTICA DIOICA (UNII: 710FLW4U46) (Active Moiety)
Which are Scalp Dermatitis 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:
- PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)
- POMEGRANATE SEED OIL (UNII: 0UI45XV0T6)
- MELALEUCA QUINQUENERVIA LEAF OIL (UNII: 22K2F1YSHD)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- SESAME OIL (UNII: QX10HYY4QV)
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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".