NDC 60914-001 Soothing First Aid 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:
Proprietary Name:
Soothing First Aid Cream
Product Type: [3]
Labeler Name: [5]
Homeo Health, Inc.
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Structure:
Code Navigator:

Product Packages

NDC Code 60914-001-00

Package Description: 14 g in 1 TUBE

NDC Code 60914-001-01

Package Description: 50 g in 1 TUBE

NDC Code 60914-001-02

Package Description: 95 g in 1 TUBE

Product Details

What is NDC 60914-001?

The NDC code 60914-001 is assigned by the FDA to the product Soothing First Aid Cream which is product labeled by Homeo Health, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 60914-001-00 14 g in 1 tube , 60914-001-01 50 g in 1 tube , 60914-001-02 95 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 Soothing First Aid Cream?

Directions: For topical use only. Apply a small amount to affected area 3 times a day or as directed by a health care professional.

Which are Soothing First Aid Cream UNII Codes?

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

Which are Soothing First Aid 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".