1. Home
  2. Labeler Index
  3. Energique, Inc.
  4. NDC Product Code: 44911-0639 Care And Comfort Cream

NDC 44911-0639 Care And Comfort Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0639?
  4. Care And Comfort Cream 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:
44911-0639
Proprietary Name:
Care And Comfort Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Energique, Inc.
Labeler Code:
44911
Product Label ID:
ac8ee81f-0af4-46d4-b63f-beeb7d120f80
Start Marketing Date: [9]
05-12-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 44911-0639-1

Package Description: 57 g in 1 TUBE

Product Details

What is NDC 44911-0639?

The NDC code 44911-0639 is assigned by the FDA to the product Care And Comfort Cream which is product labeled by Energique, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44911-0639-1 57 g in 1 tube . 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 Care And Comfort Cream?

May temporarily relieve pain, soreness, swelling, stiffness, and symptoms of minor injuries.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve pain, soreness, swelling, stiffness, and symptoms of minor injuries.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Which are Care And Comfort Cream UNII Codes?

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

  • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
  • ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
  • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
  • MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)
  • MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (Active Moiety)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
  • HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)
  • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
  • PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI)
  • PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
  • COMFREY ROOT (UNII: M9VVZ08EKQ)
  • COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)

Which are Care And Comfort Cream 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".