NDC 56062-711 Publix Burn Relief Aloe Vera

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:
56062-711
Proprietary Name:
Publix Burn Relief Aloe Vera
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Publix Super Markets Inc
Labeler Code:
56062
Start Marketing Date: [9]
07-12-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 56062-711-19

Package Description: 226 g in 1 BOTTLE, PLASTIC

Product Details

What is NDC 56062-711?

The NDC code 56062-711 is assigned by the FDA to the product Publix Burn Relief Aloe Vera which is product labeled by Publix Super Markets Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 56062-711-19 226 g in 1 bottle, plastic . 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 Publix Burn Relief Aloe Vera?

Adults and children 2 years of age and older: apply to affected areas not more than 3 to 4 times dailychildren under 2 years of age: do not use, ask a doctor

Which are Publix Burn Relief Aloe Vera UNII Codes?

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

Which are Publix Burn Relief Aloe Vera 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:

What is the NDC to RxNorm Crosswalk for Publix Burn Relief Aloe Vera?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".