NDC 63083-7306 Sixth Chakra (third Eye) 7306
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-7306?
What are the uses for Sixth Chakra (third Eye) 7306?
Which are Sixth Chakra (third Eye) 7306 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)
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SPIGELIA ANTHELMIA WHOLE (UNII: WYT05213GE)
- SPIGELIA ANTHELMIA WHOLE (UNII: WYT05213GE) (Active Moiety)
- BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q)
- BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q) (Active Moiety)
- LYCOSA TARANTULA (UNII: 86M454L2TT)
- LYCOSA TARANTULA (UNII: 86M454L2TT) (Active Moiety)
- CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE)
- CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE) (Active Moiety)
- CALCIUM HEXAFLUOROSILICATE (UNII: 2NVP93XVQ3)
- CALCIUM HEXAFLUOROSILICATE (UNII: 2NVP93XVQ3) (Active Moiety)
Which are Sixth Chakra (third Eye) 7306 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".