NDC 11822-3788 Icy Hot With Lidocaine No-mess

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:
11822-3788
Proprietary Name:
Icy Hot With Lidocaine No-mess
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rite Aid Hdgrts Corp
Labeler Code:
11822
Start Marketing Date: [9]
09-30-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11822-3788-9

Package Description: 70.8 g in 1 BOTTLE

Product Details

What is NDC 11822-3788?

The NDC code 11822-3788 is assigned by the FDA to the product Icy Hot With Lidocaine No-mess which is product labeled by Rite Aid Hdgrts Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11822-3788-9 70.8 g in 1 bottle . 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 Icy Hot With Lidocaine No-mess?

Adults and children over 12 years:■ apply a thin layer to affected area not more than 3 to 4 times daily■ massage into painful area until thoroughly absorbed into skin■ IF MEDICINE COMES IN CONTACT WITH HANDS, WASH WITH SOAP AND WATERchildren 12 years or younger: ask a doctor

Which are Icy Hot With Lidocaine No-mess UNII Codes?

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

Which are Icy Hot With Lidocaine No-mess 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".