NDC 69822-101 Ice Quake Plus

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:
69822-101
Proprietary Name:
Ice Quake Plus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
69822
Start Marketing Date: [9]
01-01-2013
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 69822-101?

The NDC code 69822-101 is assigned by the FDA to the product Ice Quake Plus which is product labeled by Southern Sales & Service, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69822-101-04 113 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 Ice Quake Plus?

adults and children over 18 years and older:Apply to affected areaSqueeze desired amount of IceQuake Plus onto affected areamassage dispensed cream into painful area until thoroughly absorbedRepeat as necessary, but no more than 3 to 4 times daily

Which are Ice Quake Plus UNII Codes?

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

Which are Ice Quake Plus 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 Ice Quake Plus?

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:
  • RxCUI: 1990885 - camphor 3.1 % / menthol 10 % / methyl salicylate 10 % Topical Cream
  • RxCUI: 1990885 - camphor 31 MG/ML / menthol 100 MG/ML / methyl salicylate 100 MG/ML Topical Cream
  • RxCUI: 1990890 - Ice Quake 3.1 % / 10 % / 10 % Topical Cream
  • RxCUI: 1990890 - camphor 31 MG/ML / menthol 100 MG/ML / methyl salicylate 100 MG/ML Topical Cream [Ice Quake]
  • RxCUI: 1990890 - Ice Quake (camphor 3.1 % / menthol 10 % / methyl salicylate 10 % ) Topical Cream

* 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".