NDC 68703-089 Mucus-clear
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68703 - Native Remedies, Llc
- 68703-089 - Mucus-clear
Product Packages
NDC Code 68703-089-59
Package Description: 59 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 68703-089?
What are the uses for Mucus-clear?
Which are Mucus-clear UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- POTASSIUM SULFATE (UNII: 1K573LC5TV)
- SULFATE ION (UNII: 7IS9N8KPMG) (Active Moiety)
Which are Mucus-clear 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)
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[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".