NDC 10578-020 Homeopathic Rheumatism
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10578 - Indiana Botanic Gardens
- 10578-020 - Homeopathic Rheumatism
Product Characteristics
Product Packages
NDC Code 10578-020-01
Package Description: 28 g in 1 JAR
Product Details
What is NDC 10578-020?
What are the uses for Homeopathic Rheumatism?
Which are Homeopathic Rheumatism UNII Codes?
The UNII codes for the active ingredients in this product are:
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB)
- RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
Which are Homeopathic Rheumatism 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:
- WATER (UNII: 059QF0KO0R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- TRICAPRYLIN (UNII: 6P92858988)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MINERAL OIL (UNII: T5L8T28FGP)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER 934 (UNII: Z135WT9208)
- IMIDUREA (UNII: M629807ATL)
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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".