NDC 64249-0003 Esmenopa
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64249 - Vitamed, Llc
- 64249-0003 - Esmenopa
Product Packages
NDC Code 64249-0003-1
Package Description: 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 64249-0003?
What are the uses for Esmenopa?
Which are Esmenopa UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHASTE TREE (UNII: 433OSF3U8A)
- CHASTE TREE (UNII: 433OSF3U8A) (Active Moiety)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- AMERICAN GINSENG (UNII: 8W75VCV53Q)
- AMERICAN GINSENG (UNII: 8W75VCV53Q) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- GALIUM APARINE (UNII: Z4B6561488)
- GALIUM APARINE (UNII: Z4B6561488) (Active Moiety)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (Active Moiety)
- SUS SCROFA OVARY (UNII: S7YTV04R8O)
- SUS SCROFA OVARY (UNII: S7YTV04R8O) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (Active Moiety)
Which are Esmenopa 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".