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NDC 68703-354 Behavior-rite

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68703-354?
  5. Behavior-rite Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68703-354
Proprietary Name:
Behavior-rite
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Silver Star Brands
Labeler Code:
68703
Product Label ID:
b78dbf3f-33fc-8613-e053-2a95a90ac7c2
Start Marketing Date: [9]
01-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
NONE
Score:
1

Product Packages

NDC Code 68703-354-80

Package Description: 180 TABLET in 1 BOTTLE, GLASS

Product Details

What is NDC 68703-354?

The NDC code 68703-354 is assigned by the FDA to the product Behavior-rite which is product labeled by Silver Star Brands. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68703-354-80 180 tablet in 1 bottle, glass . 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 Behavior-rite?

Directions: Chew or dissolve tablets in the mouth. Alternatively crush and sprinkle directly on the tongue or mix in warm waater or soft food. Use 3 times daily until symptoms improve. Adults and children 13+: 2 tablets. Children 2-12: 1 tablet.

Which are Behavior-rite UNII Codes?

The UNII codes for the active ingredients in this product are:

  • ARTEMISIA MARITIMA FLOWER (UNII: 6654882GP8)
  • ARTEMISIA MARITIMA FLOWER (UNII: 6654882GP8) (Active Moiety)
  • CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
  • CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17) (Active Moiety)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
  • VIOLA TRICOLOR (UNII: 9Q24RAI43V)
  • VIOLA TRICOLOR (UNII: 9Q24RAI43V) (Active Moiety)
  • ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E)
  • ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E) (Active Moiety)

Which are Behavior-rite 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".