Arizona Sun Sunscreen Spf15 Lotion
NDC Package 61973-101-04
Package Information
Arizona Sun Sunscreen Spf15 (sunscreen) lotions is apply liberally and evenly to the skin 30 minutes before and during sun exposure. This formulation utilizes a lotion delivery system. Marketed by Arizona Sun, this product is identified by NDC 61973-101 and is authorized under FDA application M020.
Identification & Billing
Clinical Specifications
- Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
- Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
- Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
- Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
- AVOBENZONE 20 mg/g
- OCTINOXATE 75 mg/g
- OCTISALATE 30 mg/g
- OXYBENZONE 30 mg/g
- AVOBENZONE 20 mg/g
- OCTINOXATE 75 mg/g
- OCTISALATE 30 mg/g
- OXYBENZONE 30 mg/g
- AVOBENZONE 20 mg/g
- OCTINOXATE 75 mg/g
- OCTISALATE 30 mg/g
- OXYBENZONE 30 mg/g
- AVOBENZONE 20 mg/g
- OCTINOXATE 75 mg/g
- OCTISALATE 30 mg/g
- OXYBENZONE 30 mg/g
Regulatory & Marketing
Hierarchy Structure
- 61973 - Arizona Sun
- 61973-101 - Arizona Sun Sunscreen Spf15
- 61973-101-04 - 120 g in 1 BOTTLE
- 61973-101 - Arizona Sun Sunscreen Spf15
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (61973-101). Click a package code to view its specific billing and regulatory data.
* 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 61973-101-04 identifies a specific commercial package of 120 g in 1 bottle of Arizona Sun Sunscreen Spf15, a human over the counter drug labeled by Arizona Sun. This lotion is formulated for topical use and contains avobenzone; octinoxate; octisalate; 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 Arizona Sun on February 05, 2024. The current certification is valid through December 31, 2027.
How is this Arizona Sun product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 61973010104. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.