NDC 55413-2500 Raw Ice

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:
55413-2500
Proprietary Name:
Raw Ice
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Raw Health International, Llc
Labeler Code:
55413
Start Marketing Date: [9]
01-15-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 55413-2500-1

Package Description: .089 L in 1 BOTTLE

NDC Code 55413-2500-2

Package Description: .118 L in 1 BOTTLE

NDC Code 55413-2500-3

Package Description: .004 L in 1 PACKET

Product Details

What is NDC 55413-2500?

The NDC code 55413-2500 is assigned by the FDA to the product Raw Ice which is product labeled by Raw Health International, Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 55413-2500-1 .089 l in 1 bottle , 55413-2500-2 .118 l in 1 bottle , 55413-2500-3 .004 l in 1 packet . 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 Raw Ice?

For adults and children 6 years of age and older: Shake well. Clean skin. Apply a liberal amount of gel directly on the skin over the affected area until absorbed into skin. Repeat as necessary, but not more than 4 times daily. May also be applied before or after activity. For children under 6 years of age, consult a health care professional.

Which are Raw Ice UNII Codes?

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

Which are Raw Ice 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 Raw Ice?

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".