NDC 63083-7306 Sixth Chakra (third Eye) 7306

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63083-7306
Proprietary Name:
Sixth Chakra (third Eye) 7306
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
63083
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 63083-7306?

The NDC code 63083-7306 is assigned by the FDA to the product Sixth Chakra (third Eye) 7306 which is product labeled by Professional Complementary Health Formulas. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63083-7306-1 29.5 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Sixth Chakra (third Eye) 7306?

Temporarily relieves heightened skepticism, being judgmental or dismissive, being detached from others, not trusting ones self, being focused inward, fear of the unknown, sadness, indecisiveness, or procrastination.*

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:

* Please review the disclaimer below.

Product Footnotes

[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".