NDC 63083-2104 Lung Formula 2104
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2104 - Lung Formula
Product Packages
NDC Code 63083-2104-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2104?
What are the uses for Lung Formula 2104?
Which are Lung Formula 2104 UNII Codes?
The UNII codes for the active ingredients in this product are:
- STEMONA TUBEROSA ROOT (UNII: 7S9328671Z)
- STEMONA TUBEROSA ROOT (UNII: 7S9328671Z) (Active Moiety)
- GLYCYRRHIZA INFLATA ROOT (UNII: 1MV1Z7MKVQ)
- GLYCYRRHIZA INFLATA ROOT (UNII: 1MV1Z7MKVQ) (Active Moiety)
- TRICHOSANTHES KIRILOWII SEED (UNII: 4P83085QFM)
- TRICHOSANTHES KIRILOWII SEED (UNII: 4P83085QFM) (Active Moiety)
- LAMINARIA JAPONICA (UNII: WE98HW412B)
- LAMINARIA JAPONICA (UNII: WE98HW412B) (Active Moiety)
- PUMICE (UNII: NT5NN5KL16)
- PUMICE (UNII: NT5NN5KL16) (Active Moiety)
- SARGASSUM PALLIDUM (UNII: 074P18919S)
- SARGASSUM PALLIDUM (UNII: 074P18919S) (Active Moiety)
- IMPERATA CYLINDRICA ROOT (UNII: VYT2JA85NH)
- IMPERATA CYLINDRICA ROOT (UNII: VYT2JA85NH) (Active Moiety)
- MORUS ALBA LEAF (UNII: M8YIA49Q2P)
- MORUS ALBA LEAF (UNII: M8YIA49Q2P) (Active Moiety)
- DESCURAINIA SOPHIA SEED (UNII: 2GYP0LIJ8Z)
- DESCURAINIA SOPHIA SEED (UNII: 2GYP0LIJ8Z) (Active Moiety)
- PRUNUS ARMENIACA SEED (UNII: 75356789IW)
- PRUNUS ARMENIACA SEED (UNII: 75356789IW) (Active Moiety)
- ALPINIA OXYPHYLLA FRUIT (UNII: 1QBV21VOZI)
- ALPINIA OXYPHYLLA FRUIT (UNII: 1QBV21VOZI) (Active Moiety)
- HOUTTUYNIA CORDATA WHOLE (UNII: O3E12ZLW5T)
- HOUTTUYNIA CORDATA WHOLE (UNII: O3E12ZLW5T) (Active Moiety)
Which are Lung Formula 2104 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
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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".