Lucky Super Soft Antifungal
NDC Package 72119-001-85
Package Information
Lucky Super Soft Antifungal is ■ wash affected area and dry thoroughly ■ shake can well and spray a thin layer over affected area twice daily (morning and night) ■ supervise children in the use of this product ■ for athlete's foot, pay special attention to spaces between the toes, wear well-fitting, ventilated shoes and change shoes and socks at least once a day ■ use daily for 4 weeks, if conditions persist longer, ask a doctor ■ to prevent athlete's foot, apply once or twice daily (morning and/or night) ■ this product is not effective on the scalp or nails ■ in case of clogging, clean nozzle with pin. Marketed by Blue Sea Aerosol & Daily Care Co.,ltd, this product is identified by NDC 72119-001 and is authorized under FDA application part333C.
Identification & Billing
- RxCUI: 705934 - tolnaftate 1 % Powder Spray
- RxCUI: 705934 - tolnaftate 0.01 MG/MG Powder Spray
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 72119 - Blue Sea Aerosol & Daily Care Co.,ltd
- 72119-001 - Lucky Super Soft Antifungal
- 72119-001-85 - 85 g in 1 CAN
- 72119-001 - Lucky Super Soft Antifungal
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 (72119-001). 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 72119-001-85 identifies a specific commercial package of 85 g in 1 can of Lucky Super Soft Antifungal For Athletes Foot, labeled by Blue Sea Aerosol & Daily Care Co.,ltd. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Blue Sea Aerosol & Daily Care Co.,ltd on February 19, 2018. The current certification is valid through December 31, 2021.
How is this Blue Sea Aerosol & Daily Care Co.,ltd product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 72119000185. 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.