NDC 69008-4040 Combination Remedy 40 - Allergies Hay Fever

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:
69008-4040
Proprietary Name:
Combination Remedy 40 - Allergies Hay Fever
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Warsan Homoeopathic Laboratories
Labeler Code:
69008
Start Marketing Date: [9]
11-15-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69008-4040-1

Package Description: 20 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 69008-4040?

The NDC code 69008-4040 is assigned by the FDA to the product Combination Remedy 40 - Allergies Hay Fever which is product labeled by Warsan Homoeopathic Laboratories. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69008-4040-1 20 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 Combination Remedy 40 - Allergies Hay Fever?

Temporary relief from seasonal allergies, excessive nasal discharge, itching and congestion.

Which are Combination Remedy 40 - Allergies Hay Fever UNII Codes?

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

  • EUPHRASIA STRICTA (UNII: C9642I91WL)
  • EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
  • POTASSIUM DICHROMATE (UNII: T4423S18FM)
  • DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
  • SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
  • SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
  • SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
  • SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)

Which are Combination Remedy 40 - Allergies Hay Fever 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:

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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".