NDC 50845-0247 Cold Plus Flu

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:
50845-0247
Proprietary Name:
Cold Plus Flu
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Liddell Laboratories, Inc.
Labeler Code:
50845
Start Marketing Date: [9]
01-15-2019
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50845-0247-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 50845-0247?

The NDC code 50845-0247 is assigned by the FDA to the product Cold Plus Flu which is product labeled by Liddell Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50845-0247-1 30 ml in 1 bottle, spray . 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 Cold Plus Flu?

Adults and children over 12: Spray twice under the tongue three times per day. For severe symptoms, dosage may be taken up to six times the first day.Children 12 and under: Consult a doctor prior to use.

Which are Cold Plus Flu UNII Codes?

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

  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)
  • ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
  • ANTIMONY CATION (3+) (UNII: 069647RPT5) (Active Moiety)
  • APIS MELLIFERA (UNII: 7S82P3R43Z)
  • APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • SUS SCROFA LUNG (UNII: 7GL3G1COB3)
  • SUS SCROFA LUNG (UNII: 7GL3G1COB3) (Active Moiety)
  • SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U)
  • SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (Active Moiety)
  • ANGUILLA ROSTRATA BLOOD SERUM (UNII: L7B16ESD1U)
  • ANGUILLA ROSTRATA BLOOD SERUM (UNII: L7B16ESD1U) (Active Moiety)
  • LOBARIA PULMONARIA (UNII: D1YM0P5Z2T)
  • LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (Active Moiety)

Which are Cold Plus Flu 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".