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  4. NDC Product Code: 63083-9314 Chlorinated Ring Combination 9314

NDC 63083-9314 Chlorinated Ring Combination 9314

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63083-9314?
  4. Chlorinated Ring Combination 9314 Uses
  5. Active Ingredients UNII Codes
  6. 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:
63083-9314
Proprietary Name:
Chlorinated Ring Combination 9314
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Professional Complementary Health Formulas
Labeler Code:
63083
Product Label ID:
2d75c97c-7b44-421a-b017-d011b3a31617
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63083-9314-1

Package Description: 29.5 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 63083-9314?

The NDC code 63083-9314 is assigned by the FDA to the product Chlorinated Ring Combination 9314 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 63083-9314-1 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 Chlorinated Ring Combination 9314?

For the temporary relief of occasional headache, upper respiratory irritation, nausea or vomiting, red or irritated skin or eyes, or weakness.*

Which are Chlorinated Ring Combination 9314 UNII Codes?

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

  • BLACK COHOSH (UNII: K73E24S6X9)
  • BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN)
  • CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN) (Active Moiety)
  • ACETIC ACID, (2,4,5-TRICHLOROPHENOXY)-, 2-ETHYL-4-METHYLPENTYL ESTER (UNII: 03HP3QF78W)
  • ACETIC ACID, (2,4,5-TRICHLOROPHENOXY)-, 2-ETHYL-4-METHYLPENTYL ESTER (UNII: 03HP3QF78W) (Active Moiety)
  • HEXACHLOROBENZENE (UNII: 4Z87H0LKUY)
  • HEXACHLOROBENZENE (UNII: 4Z87H0LKUY) (Active Moiety)
  • PENTACHLOROPHENOL (UNII: D9BSU0SE4T)
  • PENTACHLOROPHENOL (UNII: D9BSU0SE4T) (Active Moiety)
  • FENSON (UNII: DFC2HB4I0K)
  • FENSON (UNII: DFC2HB4I0K) (Active Moiety)

Which are Chlorinated Ring Combination 9314 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".