Noveha Nighttime Gel
NDC Package 84008-004-02

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

Package Information

Noveha Nighttime (white petrolatum) gel is uses:For temporary relief of burning and irritation due to dryness of the eye.For use as a lubricant to prevent further irritation or to relieve dryness of the eyeWhen using this productDo not touch tip of container to any surface to avoid contamination.Replace cap after use. This formulation utilizes a gel delivery system. Marketed by Bullet Point Llc, this product is identified by NDC 84008-004 and is authorized under FDA application M018.

Identification & Billing

NDC Package Code
84008-004-02
Package Description
1 TUBE in 1 BOX / 10 g in 1 TUBE
Product Code
84008-004
11-Digit Billing Format
84008000402

Clinical Specifications

Proprietary Name
Noveha Nighttime
Non-Proprietary Name
White Petrolatum
Substance Name
Light Mineral Oil; White Petrolatum
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route
Ophthalmic - Administration to the external eye.
Active Ingredient(s)
Usage Information
Uses:For temporary relief of burning and irritation due to dryness of the eye.For use as a lubricant to prevent further irritation or to relieve dryness of the eyeWhen using this productDo not touch tip of container to any surface to avoid contamination.Replace cap after use

Regulatory & Marketing

Labeler Name
Bullet Point Llc
Product Type
Human Otc Drug
FDA Application #
M018
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-22-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 84008-004-02 identifies a specific commercial package of 1 tube in 1 box / 10 g in 1 tube of Noveha Nighttime, a human over the counter drug labeled by Bullet Point Llc. This gel is formulated for ophthalmic use and contains light mineral oil; white 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 Bullet Point Llc on March 22, 2026. The current certification is valid through December 31, 2027.

How is this Bullet Point Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84008000402. 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)
84008-004-02
11-Digit CMS (5-4-2)
84008-0004-02

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