NDC 60681-2802 Pleo Poly D
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60681 - Sanum Kehlbeck Gmbh & Co. Kg
- 60681-2802 - Pleo Poly D
Product Packages
NDC Code 60681-2802-1
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 60681-2802?
What are the uses for Pleo Poly D?
Which are Pleo Poly D UNII Codes?
The UNII codes for the active ingredients in this product are:
- LACTOCOCCUS LACTIS IMMUNOSERUM RABBIT (UNII: AST1Y049U1)
- LACTOCOCCUS LACTIS IMMUNOSERUM RABBIT (UNII: AST1Y049U1) (Active Moiety)
- STREPTOCOCCUS PYOGENES IMMUNOSERUM RABBIT (UNII: 726RS6QMS8)
- STREPTOCOCCUS PYOGENES IMMUNOSERUM RABBIT (UNII: 726RS6QMS8) (Active Moiety)
- STREPTOCOCCUS VIRIDANS GROUP IMMUNOSERUM RABBIT (UNII: 4U4OEA495W)
- STREPTOCOCCUS VIRIDANS GROUP IMMUNOSERUM RABBIT (UNII: 4U4OEA495W) (Active Moiety)
- STAPHYLOCOCCUS EPIDERMIDIS IMMUNOSERUM RABBIT (UNII: 8409DJA34Y)
- STAPHYLOCOCCUS EPIDERMIDIS IMMUNOSERUM RABBIT (UNII: 8409DJA34Y) (Active Moiety)
- STAPHYLOCOCCUS AUREUS IMMUNOSERUM RABBIT (UNII: Q1G8TGQ05J)
- STAPHYLOCOCCUS AUREUS IMMUNOSERUM RABBIT (UNII: Q1G8TGQ05J) (Active Moiety)
- STREPTOCOCCUS PNEUMONIAE IMMUNOSERUM RABBIT (UNII: IWJ46H2H5C)
- STREPTOCOCCUS PNEUMONIAE IMMUNOSERUM RABBIT (UNII: IWJ46H2H5C) (Active Moiety)
- MYCOBACTERIUM BOVIS IMMUNOSERUM RABBIT (UNII: NNW4543CRP)
- MYCOBACTERIUM BOVIS IMMUNOSERUM RABBIT (UNII: NNW4543CRP) (Active Moiety)
Which are Pleo Poly D 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)
* 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".