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  4. NDC Product Code: 50845-0277 Insect Bites

NDC 50845-0277 Insect Bites

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50845-0277?
  4. Insect Bites 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:
50845-0277
Proprietary Name:
Insect Bites
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Liddell Laboratories, Inc.
Labeler Code:
50845
Product Label ID:
f7b30297-0710-4319-b4ee-df485832d64d
Start Marketing Date: [9]
07-16-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 50845-0277?

The NDC code 50845-0277 is assigned by the FDA to the product Insect Bites 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 50845-0277-1 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 Insect Bites?

May temporarily relieve symptoms associated with insect bites or stings: redness, swelling, itching, soreness.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve symptoms associated with insect bites or stings: redness, swelling, itching, soreness.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Which are Insect Bites UNII Codes?

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

  • BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N)
  • BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N) (Active Moiety)
  • APIS MELLIFERA (UNII: 7S82P3R43Z)
  • APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
  • ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
  • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
  • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
  • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
  • ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
  • EUPHORBIA HIRTA FLOWERING TOP (UNII: 6H89ZY31MR)
  • EUPHORBIA HIRTA FLOWERING TOP (UNII: 6H89ZY31MR) (Active Moiety)
  • GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI)
  • GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI) (Active Moiety)
  • HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
  • HISTAMINE (UNII: 820484N8I3) (Active Moiety)
  • HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)
  • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
  • LACHESIS MUTA VENOM (UNII: VSW71SS07I)
  • LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
  • LATRODECTUS MACTANS (UNII: XJJ7QA858R)
  • LATRODECTUS MACTANS (UNII: XJJ7QA858R) (Active Moiety)
  • RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P)
  • LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
  • RANCID BEEF (UNII: 29SUH5R3HU)
  • RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
  • CITHARACANTHUS SPINICRUS (UNII: 3Y5X6RT823)
  • CITHARACANTHUS SPINICRUS (UNII: 3Y5X6RT823) (Active Moiety)

Which are Insect Bites 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".