NDC 44911-0278 Postpituapar
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 44911 - Energique, Inc.
- 44911-0278 - Postpituapar
Product Packages
NDC Code 44911-0278-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 44911-0278?
What are the uses for Postpituapar?
Which are Postpituapar UNII Codes?
The UNII codes for the active ingredients in this product are:
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K)
- BOS TAURUS PITUITARY GLAND (UNII: 7JM57I419K) (Active Moiety)
- PULSATILLA PRATENSIS (UNII: 8E272251DI)
- PULSATILLA PRATENSIS (UNII: 8E272251DI) (Active Moiety)
- SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U)
- SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
Which are Postpituapar 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)
- ALCOHOL (UNII: 3K9958V90M)
* 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".