NDC 59555-601 I.c. Barrier

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:
59555-601
Proprietary Name:
I.c. Barrier
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
R&r Lotion, Inc.
Labeler Code:
59555
Start Marketing Date: [9]
09-17-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 59555-601-04

Package Description: 60 mL in 1 BOTTLE, PUMP

NDC Code 59555-601-08

Package Description: 237 mL in 1 BOTTLE, PUMP

NDC Code 59555-601-10

Package Description: 946 mL in 1 BOTTLE, PUMP

NDC Code 59555-601-11

Package Description: 3785 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 59555-601?

The NDC code 59555-601 is assigned by the FDA to the product I.c. Barrier which is product labeled by R&r Lotion, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 59555-601-04 60 ml in 1 bottle, pump , 59555-601-08 237 ml in 1 bottle, pump , 59555-601-10 946 ml in 1 bottle, pump , 59555-601-11 3785 ml in 1 bottle, pump . 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 I.c. Barrier?

Apply to hands & body and rub until lotion is absorbed. Will not dry out your skin or crack your nails like Alcohol Based Sanitizers.

Which are I.c. Barrier UNII Codes?

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

Which are I.c. Barrier 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 I.c. Barrier?

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: 1549533 - benzethonium chloride 0.2 % / dimethicone 2 % Topical Lotion
  • RxCUI: 1549533 - benzethonium chloride 2 MG/ML / dimethicone 20 MG/ML Topical Lotion

* 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".