Critic-aid Clear Ointment
NDC Package 11701-083-32

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Critic-aid Clear (petrolatum) ointment is 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. This formulation utilizes a ointment delivery system. Marketed by Coloplast Corp, this product is identified by NDC 11701-083 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
11701-083-32
Package Description
170 g in 1 TUBE
Product Code
11701-083
11-Digit Billing Format
11701008332
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Critic-aid Clear
Non-Proprietary Name
Petrolatum
Substance Name
Petrolatum
Dosage Form
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
PETROLATUM 865 mg/g
Usage Information
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.

Regulatory & Marketing

Labeler Name
Coloplast Corp
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-22-2019
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (11701-083). Click a package code to view its specific billing and regulatory data.

11701-083-22
4 g in 1 PACKET
11701-083-33
71 g in 1 TUBE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 11701-083-32 identifies a specific commercial package of 170 g in 1 tube of Critic-aid Clear, a human over the counter drug labeled by Coloplast Corp. This ointment is formulated for topical use and contains petrolatum as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Coloplast Corp on January 22, 2019. The current certification is valid through December 31, 2027.

How is this Coloplast Corp product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11701008332. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
11701-083-32
11-Digit CMS (5-4-2)
11701-0083-32

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.