Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum Spf 30 Lotion
NDC Package 52328-301-01
Package Information
Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum Spf 30 (titanium dioxide, zinc oxide) lotions is shake bottle well before use.• For Sunscreen Use:• apply generously 15 minutes before sun exposure• reapply:• after 80 minutes of swimming or sweating• immediately after towel drying• at least every 2 hours• Sun Protection Measures.Spending time in the sun increases your risk of skin cancer and early skin aging. This formulation utilizes a lotion delivery system. Marketed by Acupac Packaging, Inc., this product is identified by NDC 52328-301 and is authorized under FDA application M020.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 52328 - Acupac Packaging, Inc.
- 52328-301 - Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum Spf 30
- 52328-301-01 - 24 POUCH in 1 CARTON / .05 mL in 1 POUCH
- 52328-301 - Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum Spf 30
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.
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Other Available Packages
The following commercial packages are registered under the same Product NDC (52328-301). Click a package code to view its specific billing and regulatory data.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 52328-301-01 identifies a specific commercial package of 24 pouch in 1 carton / .05 ml in 1 pouch of Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum Spf 30, a human over the counter drug labeled by Acupac Packaging, Inc.. This lotion is formulated for topical use and contains titanium dioxide; zinc oxide 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 Acupac Packaging, Inc. on August 21, 2023. The current certification is valid through December 31, 2027.
How is this Acupac Packaging, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 52328030101. 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.