NDC 60512-0018 Headache/migraine Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60512 - Homeolab Usa Inc.
- 60512-0018 - Headache/migraine Relief
Product Characteristics
Product Packages
NDC Code 60512-0018-1
Package Description: 80 PELLET in 1 TUBE
Product Details
What is NDC 60512-0018?
What are the uses for Headache/migraine Relief?
Which are Headache/migraine Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- CYCLAMEN PURPURASCENS TUBER (UNII: G728143D8Q)
- CYCLAMEN PURPURASCENS TUBER (UNII: G728143D8Q) (Active Moiety)
- ANTIMONY TRISULFIDE (UNII: F79059A38U)
- ANTIMONY TRISULFIDE (UNII: F79059A38U) (Active Moiety)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM OXIDE (UNII: LMI26O6933) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- DIGITALIS PURPUREA WHOLE (UNII: UD4O8TY7RW)
- DIGITALIS PURPUREA WHOLE (UNII: UD4O8TY7RW) (Active Moiety)
- MELILOTUS OFFICINALIS TOP (UNII: GM6P02J2DX)
- MELILOTUS OFFICINALIS TOP (UNII: GM6P02J2DX) (Active Moiety)
- NITROGLYCERIN (UNII: G59M7S0WS3)
- NITROGLYCERIN (UNII: G59M7S0WS3) (Active Moiety)
Which are Headache/migraine 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".