Hydrocortisone Cream 1%
NDC Package 70512-101-30

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Hydrocortisone Cream 1% is adults and children over 2 years of age - Apply to affected area not more than 3-4 times per day. Marketed by Sola Pharmaceuticals, this product is identified by NDC 70512-101 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
70512-101-30
Package Description
1 TUBE in 1 CARTON / 30 g in 1 TUBE
Product Code
70512-101
11-Digit Billing Format
70512010130
Billing Unit
GM - Billing unit of "gram" is used when a product is measured by its weight.
Units Per Package
30 GM
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Hydrocortisone Cream 1%
Dosage Form
-
Usage Information
Adults and children over 2 years of age - Apply to affected area not more than 3-4 times per day. Children under 2 years of age - Do not use. Consult a doctor. For external anal itching Adults - When practical cleanse the affcted area with mild soap and water and rinse thoroughly. Gently dry patting with bathroom tissue or soft cloth before applying. ​Apply to affected area not more than 3-4 times per day. Children under 12 years of age: consult a doctor.

Regulatory & Marketing

Labeler Name
Sola Pharmaceuticals
FDA Application #
part348
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
04-16-2020
Listing Expiration
12-31-2023
Exclude Flag
I
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 70512-101-30 identifies a specific commercial package of 1 tube in 1 carton / 30 g in 1 tube of Hydrocortisone Cream 1%, labeled by Sola Pharmaceuticals. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Sola Pharmaceuticals on April 16, 2020. The current certification is valid through December 31, 2023.

How is this Sola Pharmaceuticals product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70512010130. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. There are 30 total billable units per package. 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)
70512-101-30
11-Digit CMS (5-4-2)
70512-0101-30

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