NDC Package 75568-036-01 Bonica Easex Pain Relieving

Camphor (synthetic),Menthol,Methyl Salicylate Patch Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
75568-036-01
Package Description:
1 POUCH in 1 BOX / 360 PATCH in 1 POUCH / .33 g in 1 PATCH
Product Code:
Proprietary Name:
Bonica Easex Pain Relieving
Non-Proprietary Name:
Camphor (synthetic), Menthol, Methyl Salicylate
Substance Name:
Camphor (synthetic); Menthol; Methyl Salicylate
Usage Information:
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
11-Digit NDC Billing Format:
75568003601
NDC to RxNorm Crosswalk:
  • 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
Product Type:
Human Otc Drug
Labeler Name:
Planet (anhui) Pharmaceutical Co., Ltd.
Dosage Form:
Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
Administration Route(s):
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Sample Package:
No
FDA Application Number:
M
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
07-01-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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 NDC 75568-036-01?

The NDC Packaged Code 75568-036-01 is assigned to a 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.. The product's dosage form is patch and is administered via topical form.

Is NDC 75568-036 included in the NDC Directory?

Yes, Bonica Easex Pain Relieving with product code 75568-036 is active and included in the NDC Directory. The product was first marketed by Planet (anhui) Pharmaceutical Co., Ltd. on July 01, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 75568-036-01?

The 11-digit format is 75568003601. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-275568-036-015-4-275568-0036-01