NDC 76509-150 Kids Cough
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76509 - Natures Investment Holdings Pty Ltd Dba Maxrelief Usa
- 76509-150 - Kids Cough
Product Packages
NDC Code 76509-150-01
Package Description: 10 LOZENGE in 1 BOX
NDC Code 76509-150-02
Package Description: 10 LOZENGE in 1 BOX
Product Details
What is NDC 76509-150?
What are the uses for Kids Cough?
Which are Kids Cough UNII Codes?
The UNII codes for the active ingredients in this product are:
- DROSERA INTERMEDIA (UNII: B3G4A96QLY)
- DROSERA INTERMEDIA (UNII: B3G4A96QLY) (Active Moiety)
- SPONGIA OFFICINALIS WHOLE (UNII: 755U7L3M7Z)
- SPONGIA OFFICINALIS WHOLE (UNII: 755U7L3M7Z) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- IPECAC (UNII: 62I3C8233L)
- IPECAC (UNII: 62I3C8233L) (Active Moiety)
Which are Kids Cough 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:
- ISOMALT (UNII: S870P55O2W)
- COCHINEAL (UNII: TZ8Z31B35M)
* 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".