NDC 63083-7301 First Chakra (root) 7301
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-7301?
What are the uses for First Chakra (root) 7301?
Which are First Chakra (root) 7301 UNII Codes?
The UNII codes for the active ingredients in this product are:
- MARSDENIA CUNDURANGO WHOLE (UNII: AT33ZFZ5A1)
- MARSDENIA CUNDURANGO WHOLE (UNII: AT33ZFZ5A1) (Active Moiety)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (Active Moiety)
- HELLEBORUS NIGER ROOT (UNII: 608DGJ6815)
- HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (Active Moiety)
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- BOS TAURUS BILE (UNII: ET3651ZLOU)
- BOS TAURUS BILE (UNII: ET3651ZLOU) (Active Moiety)
- LYCOSA TARANTULA (UNII: 86M454L2TT)
- LYCOSA TARANTULA (UNII: 86M454L2TT) (Active Moiety)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE RED (UNII: 1K09F3G675) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are First Chakra (root) 7301 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".