NDC 71798-015 Rhinodol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 71798-015?
What are the uses for Rhinodol?
Which are Rhinodol UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAPSICUM (UNII: 00UK7646FG)
- CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
Which are Rhinodol 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:
- SILVER (UNII: 3M4G523W1G)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ROSEMARY (UNII: IJ67X351P9)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- WATER (UNII: 059QF0KO0R)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- SEA SALT (UNII: 87GE52P74G)
- ALOE (UNII: V5VD430YW9)
- EUCALYPTOL (UNII: RV6J6604TK)
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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".