NDC 53173-0001 Sore Throat
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53173 - Nova Aurora Corp
- 53173-0001 - Sore Throat
Product Characteristics
Product Packages
NDC Code 53173-0001-1
Package Description: 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 53173-0001?
What are the uses for Sore Throat?
Which are Sore Throat UNII Codes?
The UNII codes for the active ingredients in this product are:
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- PLANTAGO MAJOR (UNII: W2469WNO6U)
- PLANTAGO MAJOR (UNII: W2469WNO6U) (Active Moiety)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
Which are Sore Throat 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:
- CLOVE (UNII: K48IKT5321)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- MYRRH (UNII: JC71GJ1F3L)
- SAGE (UNII: 065C5D077J)
- THYME (UNII: CW657OBU4N)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- MENTHOL (UNII: L7T10EIP3A)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
- SPEARMINT OIL (UNII: C3M81465G5)
* 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".