Bonica Easex Pain Relieving Patch
NDC Package 75568-036-01
Package Information
Bonica Easex Pain Relieving (camphor (synthetic), menthol, methyl salicylate) patches is adults and children 12 years of age and over:• Clean and dry affected area • Carefully remove backing from patch • Apply sticky side of patch to affected area • Use one patch for up to 8 hours • Discard patch after single use • Apply 1 patch at a time to affected area, not more than 3 to 4 times daily Children under 12 years of age:consult a physician. This formulation utilizes a patch delivery system. Marketed by Planet (anhui) Pharmaceutical Co., Ltd., this product is identified by NDC 75568-036 and is authorized under FDA application M.
Identification & Billing
- RxCUI: 1793147 - camphor 3.1 % / menthol 6 % / methyl salicylate 10 % Medicated Patch
- RxCUI: 1793147 - camphor 0.031 MG/MG / menthol 0.06 MG/MG / methyl salicylate 0.1 MG/MG Medicated Patch
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 75568 - Planet (anhui) Pharmaceutical Co., Ltd.
- 75568-036 - Bonica Easex Pain Relieving
- 75568-036-01 - 1 POUCH in 1 BOX / 360 PATCH in 1 POUCH / .33 g in 1 PATCH
- 75568-036 - Bonica Easex Pain 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 75568-036-01 identifies a specific commercial package of 1 pouch in 1 box / 360 patch in 1 pouch / .33 g in 1 patch of Bonica Easex Pain Relieving, a human over the counter drug labeled by Planet (anhui) Pharmaceutical Co., Ltd.. This patch is formulated for topical 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 Planet (anhui) Pharmaceutical Co., Ltd. on July 01, 2025. The current certification is valid through December 31, 2026.
How is this Planet (anhui) Pharmaceutical Co., Ltd. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 75568003601. 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.