H.e.b Aerosol, Spray
NDC Package 37808-976-37

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

H.e.b (sport spf 30 continuous spray) aerosols is apply liberally 15 minutes before sun exposurehold can 4-6 inches away from body, spray evenly to ensure complete coveragedo not spray into face. This formulation utilizes a aerosol, spray delivery system. Marketed by H.e.b, this product is identified by NDC 37808-976 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
37808-976-37
Package Description
156 g in 1 CAN
Product Code
11-Digit Billing Format
37808097637

Clinical Specifications

Proprietary Name
H.e.b Solutions Sunscreen
Non-Proprietary Name
Sport Spf 30 Continuous Spray
Substance Name
Avobenzone; Homosalate; Octisalate; Octocrylene; Oxybenzone
Dosage Form
Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.
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.
Usage Information
Apply liberally 15 minutes before sun exposurehold can 4-6 inches away from body, spray evenly to ensure complete coveragedo not spray into face. Spray into hand and apply to face.use in well ventilated, but not windy areasreapply:   • after 80 minutes of swimming or sweating   • immediately after towel drying   • at least every 2 hourschildren under 6 months of age: ask a doctorSun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad-spectrum SPF of 15 or higher and other sun protection measures including:   • limit time in the sun, especially from 10 a.m. - 2 p.m.   • wear long-sleeve shirts, pants, hats, and sunglasses

Regulatory & Marketing

Labeler Name
H.e.b
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-17-2012
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 37808-976-37 identifies a specific commercial package of 156 g in 1 can of H.e.b Solutions Sunscreen, a human over the counter drug labeled by H.e.b. This aerosol, spray is formulated for topical use and contains avobenzone; homosalate; octisalate; octocrylene; oxybenzone 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 H.e.b on February 17, 2012. The current certification is valid through December 31, 2026.

How is this H.e.b product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37808097637. 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)
37808-976-37
11-Digit CMS (5-4-2)
37808-0976-37

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