NDC 51393-7522 Rheumatoid Arthritis Pain Management
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51393 - Forces Of Nature
- 51393-7522 - Rheumatoid Arthritis Pain Management
Product Packages
NDC Code 51393-7522-1
Package Description: 1 BOTTLE, DISPENSING in 1 BOX / 11 mL in 1 BOTTLE, DISPENSING
NDC Code 51393-7522-2
Package Description: 1 BOTTLE, DISPENSING in 1 BOX / 33 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 51393-7522?
What are the uses for Rheumatoid Arthritis Pain Management?
Which are Rheumatoid Arthritis Pain Management UNII Codes?
The UNII codes for the active ingredients in this product are:
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ) (Active Moiety)
- CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH)
- CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Rheumatoid Arthritis Pain Management 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)
- PICEA MARIANA LEAF OIL (UNII: Q1J49L1A5O)
- LAVANDIN OIL (UNII: 9RES347CKG)
- MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
- EUCALYPTUS RADIATA LEAF OIL (UNII: SB9A7612BD)
- GINGER (UNII: C5529G5JPQ)
- SESAME OIL (UNII: QX10HYY4QV)
- CUPRESSUS SEMPERVIRENS WHOLE (UNII: V0IW9P606J)
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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".