NDC 51885-3353 Zeel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51885 - Biologische Heilmittel Heel
- 51885-3353 - Zeel
Product Packages
NDC Code 51885-3353-1
Package Description: 1 TUBE in 1 CARTON / 50 g in 1 TUBE
NDC Code 51885-3353-3
Package Description: 1 TUBE in 1 CARTON / 50 g in 1 TUBE
Product Details
What is NDC 51885-3353?
What are the uses for Zeel?
Which are Zeel UNII Codes?
The UNII codes for the active ingredients in this product are:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- ARNICA MONTANA ROOT (UNII: MUE8Y11327)
- ARNICA MONTANA ROOT (UNII: MUE8Y11327) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
- SOLANUM DULCAMARA STEM (UNII: IR986LE7DF)
- SOLANUM DULCAMARA STEM (UNII: IR986LE7DF) (Active Moiety)
- COENZYME A (UNII: SAA04E81UX)
- COENZYME A (UNII: SAA04E81UX) (Active Moiety)
- NADIDE (UNII: 0U46U6E8UK)
- NADIDE (UNII: 0U46U6E8UK) (Active Moiety)
- SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG)
- SODIUM (UNII: 9NEZ333N27) (Active Moiety)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y) (Active Moiety)
- SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F)
- SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (Active Moiety)
- SUS SCROFA EMBRYO (UNII: 9928MC12VO)
- SUS SCROFA EMBRYO (UNII: 9928MC12VO) (Active Moiety)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (Active Moiety)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8) (Active Moiety)
Which are Zeel 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:
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- PETROLATUM (UNII: 4T6H12BN9U)
- PARAFFIN (UNII: I9O0E3H2ZE)
* 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".