Yimimde PAIN RELIEF Gel-Patch NDC 73076-302

NDC codes

FDA NDC Directory

Product NDC (as listed)73076-302Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73076-0302Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
73076-302-01	73076030201	4 PATCH in 1 BOX (73076-302-01) / 12 g in 1 PATCHMarketed from Dec 1, 2024
73076-302-02	73076030202	8 PATCH in 1 BOX (73076-302-02) / 12 g in 1 PATCHMarketed from Dec 1, 2024

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Yimimde PAIN RELIEF Gel-Patch
Generic name (nonproprietary): lidocarine and menthol
Active ingredients: Menthol — 1 g/100gLidocaine — 4 g/100g
Dosage form: Patch
Route: Topical
Labeler: Shenzhen Ishan Technology Co., Ltd
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 1, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers: Product ID 73076-302_4aae7552-bf4b-ef55-e063-6394a90a1581SPL ID 4aae7552-bf4b-ef55-e063-6394a90a1581SPL set ID 29b4fc6d-a588-c1a4-e063-6394a90ae9ddUNII L7T10EIP3A, 98PI200987
Pharmacologic class: Amide Local Anesthetic; Antiarrhythmic

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N473076030201 followed by a unit qualifier and the quantity

Package 73076-0302-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Feb 12, 2026.

Indications (excerpt from the label)

Directions Adults and children 12 years of age and over: ● clean and dry affected area. ● apply 1 patch at a time to affected area, not morethan 3 to 4 times daily. ● remove film from patch and apply to the skin. Children under 12 years of age: consult a doctor

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)