NDC 90107-3621 After Bite Wipe

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:
90107-3621
Proprietary Name:
After Bite Wipe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Adventure Ready Brands
Labeler Code:
90107
Start Marketing Date: [9]
01-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 90107-3621-0

Package Description: 1.1 mL in 1 POUCH

NDC Code 90107-3621-1

Package Description: 4 POUCH in 1 BOX / 1.1 mL in 1 POUCH

Product Details

What is NDC 90107-3621?

The NDC code 90107-3621 is assigned by the FDA to the product After Bite Wipe which is product labeled by Adventure Ready Brands. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 90107-3621-0 1.1 ml in 1 pouch , 90107-3621-1 4 pouch in 1 box / 1.1 ml in 1 pouch. 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 After Bite Wipe?

Adults and Children 2 years and older: Apply to cleaned affected area not more than 3 times daily.Children under 2 years of age: consult a doctor.

Which are After Bite Wipe UNII Codes?

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

Which are After Bite Wipe 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 After Bite Wipe?

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: 1190560 - ethanol 50 % / lidocaine HCl 2 % Medicated Pad
  • RxCUI: 1190560 - ethanol 0.5 ML/ML / lidocaine hydrochloride 20 MG/ML Medicated Pad
  • RxCUI: 1190560 - ethanol 50 % / lidocaine hydrochloride 2 % Medicated Pad

* 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".