NDC 50810-1000 Dr. Jis Arthritis Plus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50810 - Ji Well Health Company
- 50810-1000 - Dr. Jis Arthritis Plus
Product Packages
NDC Code 50810-1000-2
Package Description: 1 TUBE in 1 BOX / 56699.04 mg in 1 TUBE
Product Details
What is NDC 50810-1000?
What are the uses for Dr. Jis Arthritis Plus?
Which are Dr. Jis Arthritis Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- METHYL SALICYLATE (UNII: LAV5U5022Y) (Active Moiety)
Which are Dr. Jis Arthritis Plus 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA (UNII: O80TY208ZW)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CLOVE OIL (UNII: 578389D6D0)
- GINGER OIL (UNII: SAS9Z1SVUK)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ORANGE OIL (UNII: AKN3KSD11B)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- THYME OIL (UNII: 2UK410MY6B)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Dr. Jis Arthritis Plus?
- RxCUI: 1045368 - camphor 3 % / menthol 12 % / methyl salicylate 15 % Topical Gel
- RxCUI: 1045368 - camphor 0.03 MG/MG / menthol 0.12 MG/MG / methyl salicylate 0.15 MG/MG Topical Gel
* Please review the disclaimer below.
[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".