NDC 43406-0027 Insomnia Hp
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43406 - Natural Creations, Inc.
- 43406-0027 - Insomnia Hp
Product Packages
NDC Code 43406-0027-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43406-0027?
What are the uses for Insomnia Hp?
Which are Insomnia Hp UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- MAGNESIUM CARBONATE (UNII: 0E53J927NA)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PASSIFLORA INCARNATA TOP (UNII: CLF5YFS11O)
- PASSIFLORA INCARNATA TOP (UNII: CLF5YFS11O) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- VALERIAN (UNII: JWF5YAW3QW)
- VALERIAN (UNII: JWF5YAW3QW) (Active Moiety)
Which are Insomnia Hp 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".