NDC 60512-0001 Pms Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60512 - Homeolab Usa Inc.
- 60512-0001 - Pms Relief
Product Characteristics
Product Packages
NDC Code 60512-0001-1
Package Description: 80 PELLET in 1 TUBE
Product Details
What is NDC 60512-0001?
What are the uses for Pms Relief?
Which are Pms Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACTAEA CIMICIFUGA ROOT (UNII: 65J267BAZT)
- ACTAEA CIMICIFUGA ROOT (UNII: 65J267BAZT) (Active Moiety)
- MERCURIC CHLORIDE (UNII: 53GH7MZT1R)
- MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
- JUNIPERUS SABINA LEAFY TWIG (UNII: Z5BEX9K2G1)
- JUNIPERUS SABINA LEAFY TWIG (UNII: Z5BEX9K2G1) (Active Moiety)
- HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T)
- HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T) (Active Moiety)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- HYOSCYAMUS NIGER WHOLE (UNII: 34412PDT5E)
- HYOSCYAMUS NIGER WHOLE (UNII: 34412PDT5E) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
Which are Pms Relief 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:
- SUCROSE (UNII: C151H8M554)
- LACTOSE (UNII: J2B2A4N98G)
* 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".