NDC 81386-001 Herbal Power Alternative Homeopathic Amazing Wound Treatment Skin Cream

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:
81386-001
Proprietary Name:
Herbal Power Alternative Homeopathic Amazing Wound Treatment Skin Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bells & More Inc
Labeler Code:
81386
Start Marketing Date: [9]
03-12-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81386-001-57

Package Description: 57 g in 1 CONTAINER

Product Details

What is NDC 81386-001?

The NDC code 81386-001 is assigned by the FDA to the product Herbal Power Alternative Homeopathic Amazing Wound Treatment Skin Cream which is product labeled by Bells & More Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81386-001-57 57 g in 1 container . 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 Herbal Power Alternative Homeopathic Amazing Wound Treatment Skin Cream?

Gently cleanse and dry area.Apply liberally to affected areas as needed.

Which are Herbal Power Alternative Homeopathic Amazing Wound Treatment Skin Cream UNII Codes?

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

  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
  • CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
  • CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) (Active Moiety)

Which are Herbal Power Alternative Homeopathic Amazing Wound Treatment Skin 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:

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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".