Hampton Sun Spf 70 Kids Spray
NDC Package 87170-021-05

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

Package Information

Hampton Sun Spf 70 Kids (avobenzone, humosalate, octisalate, octocrylene) sprays is a medication used as Sunscreen. This formulation utilizes a spray delivery system. Marketed by S&c Hampton Sun Llc, this product is identified by NDC 87170-021 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
87170-021-05
Package Description
142 g in 1 CAN
Product Code
11-Digit Billing Format
87170002105

Clinical Specifications

Proprietary Name
Hampton Sun Spf 70 Kids
Non-Proprietary Name
Avobenzone, Humosalate, Octisalate, Octocrylene
Substance Name
Avobenzone; Homosalate; Octisalate; Octocrylene
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
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
This product is used as Sunscreen. Uses ■ helps prevent sunburn

Regulatory & Marketing

Labeler Name
S&c Hampton Sun Llc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-25-2022
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 87170-021-05 identifies a specific commercial package of 142 g in 1 can of Hampton Sun Spf 70 Kids, a human over the counter drug labeled by S&c Hampton Sun Llc. This spray is formulated for topical use and contains avobenzone; homosalate; octisalate; octocrylene 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 S&c Hampton Sun Llc on June 25, 2022. The current certification is valid through December 31, 2027.

How is this S&c Hampton Sun Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87170002105. 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)
87170-021-05
11-Digit CMS (5-4-2)
87170-0021-05

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