Salonpas Deep Relieving Gel
NDC Package 55328-900-02
Package Information
Salonpas Deep Relieving (camphor, menthol, methyl salicylate) gel is adults and children 12 years of age and over:clean and dry affected areaapply a dime sized portion to the affected areamassage thoroughly until absorbed into skinapply to affected area not more than 3 to 4 times dailyChildren under 12 years of age: consult a doctor. This formulation utilizes a gel delivery system. Marketed by Hisamitsu America, Inc., this product is identified by NDC 55328-900 and is authorized under FDA application M017.
Identification & Billing
- RxCUI: 1425325 - camphor 3.1 % / menthol 10 % / methyl salicylate 15 % Topical Gel
- RxCUI: 1425325 - camphor 0.031 MG/MG / menthol 0.1 MG/MG / methyl salicylate 0.15 MG/MG Topical Gel
Clinical Specifications
- Percutaneous - Administration through the skin.
- Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
- Transdermal - Administration through the dermal layer of the skin to the systemic circulation by diffusion.
Regulatory & Marketing
Hierarchy Structure
- 55328 - Hisamitsu America, Inc.
- 55328-900 - Salonpas Deep Relieving
- 55328-900-02 - 1 TUBE in 1 BOX / 78 g in 1 TUBE
- 55328-900 - Salonpas Deep Relieving
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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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 55328-900-02 identifies a specific commercial package of 1 tube in 1 box / 78 g in 1 tube of Salonpas Deep Relieving, a human over the counter drug labeled by Hisamitsu America, Inc.. This product is billed per "GM" gram and contains an estimated amount of 78 billable units per package. This gel is formulated for percutaneous; topical; transdermal use and contains camphor (synthetic); menthol; methyl salicylate 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 Hisamitsu America, Inc. on June 01, 2013. The current certification is valid through December 31, 2026.
How is this Hisamitsu America, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 55328090002. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. There are 78 total billable units per package. 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.