NDC 51720-734 Mittiheal Natural Wound Care

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:
51720-734
Proprietary Name:
Mittiheal Natural Wound Care
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Curative Power Lab Pvt Ltd
Labeler Code:
51720
Start Marketing Date: [9]
08-15-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)

Product Packages

NDC Code 51720-734-84

Package Description: 1 POUCH in 1 BOX / 10 g in 1 POUCH (51720-734-82)

Product Details

What is NDC 51720-734?

The NDC code 51720-734 is assigned by the FDA to the product Mittiheal Natural Wound Care which is product labeled by Curative Power Lab Pvt Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51720-734-84 1 pouch in 1 box / 10 g in 1 pouch (51720-734-82). 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 Mittiheal Natural Wound Care?

Can be applied on cuts, scrapes, rashes, blisters, bug bites, minor burns, diabetic and venous ulcers, and bedsores. Calms skin and provides itch relief.

Which are Mittiheal Natural Wound Care UNII Codes?

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

  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
  • ARNICA MONTANA (UNII: O80TY208ZW)
  • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)

Which are Mittiheal Natural Wound Care 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".