Ea Eight Hour Skin Protectant Emulsion
NDC Package 10967-672-17

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

Package Information

Ea Eight Hour Skin Protectant (petrolatum) emulsions is ■ Apply liberally as often as necessary. This formulation utilizes a emulsion delivery system. Marketed by Revlon, this product is identified by NDC 10967-672 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
10967-672-17
Package Description
50 g in 1 TUBE
Product Code
10967-672
11-Digit Billing Format
10967067217

Clinical Specifications

Proprietary Name
Ea Eight Hour Skin Protectant
Non-Proprietary Name
Petrolatum
Substance Name
Petrolatum
Dosage Form
Emulsion - A dosage form consisting of a two-phase system comprised of at least two immiscible liquids1, one of which is dispersed as droplets (internal or dispersed phase) within the other liquid (external or continuous phase), generally stabilized with one or more emulsifying agents. (Note: Emulsion is used as a dosage form term unless a more specific term is applicable, e.g. cream, lotion, ointment.)
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 56.8 mg/g
Usage Information
■ Apply liberally as often as necessary

Regulatory & Marketing

Labeler Name
Revlon
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-16-2016
Listing Expiration
12-31-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 10967-672-17 identifies a specific commercial package of 50 g in 1 tube of Ea Eight Hour Skin Protectant, a human over the counter drug labeled by Revlon. This emulsion 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 Revlon on February 16, 2016. The current certification is valid through December 31, 2026.

How is this Revlon product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 10967067217. 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)
10967-672-17
11-Digit CMS (5-4-2)
10967-0672-17

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