NDC 11701-083 Critic-aid Clear

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:
11701-083
Proprietary Name:
Critic-aid Clear
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Coloplast Corp.
Labeler Code:
11701
Start Marketing Date: [9]
01-22-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - RUBS TO CLEAR)

Product Packages

NDC Code 11701-083-22

Package Description: 4 g in 1 PACKET

NDC Code 11701-083-32

Package Description: 170 g in 1 TUBE

NDC Code 11701-083-33

Package Description: 71 g in 1 TUBE

Product Details

What is NDC 11701-083?

The NDC code 11701-083 is assigned by the FDA to the product Critic-aid Clear which is product labeled by Coloplast Corp.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 11701-083-22 4 g in 1 packet , 11701-083-32 170 g in 1 tube , 11701-083-33 71 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 Critic-aid Clear?

Clean the affected area and dry thoroughly.Knead before use.Apply a thin layer liberally enough to cover yet visualize the skin.Apply to the affected area twice daily (morning and night), or as directed by a doctor.Supervise children in the use of this product.

Which are Critic-aid Clear UNII Codes?

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

Which are Critic-aid Clear 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 Critic-aid Clear?

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".