Over-the-counter drug · OTC MONOGRAPH DRUG
Pain Relief (Lidocaine) NDC 73557-189
Lidocaine .04 g/g · Patch · Topical · Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 73557-189-30 | 7355701893073557018930 | 30 BAG in 1 BOX (73557-189-30) / 1 PATCH in 1 BAG / 9 g in 1 PATCHMarketed from Nov 10, 2025 |
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)
- Pain Relief
- Generic name (nonproprietary)
- lidocaine
- Active ingredients
- Lidocaine — .04 g/g
- Dosage form
- Patch
- Route
- Topical
- Labeler
- Shanghai Chuangshi Medical Technology (Group) Co., Ltd.NDC labeler code 73557
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Other FDA classes
- Amides (Chemical structure)Local Anesthesia (Physiologic effect)
- Identifiers
- Product ID 73557-189_51d35d15-46ec-bbed-e063-6394a90a9fc3SPL ID 51d35d15-46ec-bbed-e063-6394a90a9fc3SPL set ID 433ac435-279e-574b-e063-6294a90a1d6dRxCUI 1737778UNII 98PI200987UPC 6924239707476
- 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
N473557018930followed by a unit qualifier and the quantityPackage 73557-0189-30. 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 .
Indications (excerpt from the label)
Uses For temporary relief of pain
Excerpt only. Read the full label for complete information.
About NDC 73557-189
- What is NDC 73557-189?
- 73557-189 is the product NDC for Pain Relief (lidocaine), Lidocaine .04 g/g patch, listed with the FDA by Shanghai Chuangshi Medical Technology (Group) Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Pain Relief (Lidocaine).
- What is the active ingredient?
- Lidocaine.
- Who is the labeler?
- Shanghai Chuangshi Medical Technology (Group) Co., Ltd., NDC labeler code 73557. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Pain Relief?
- 62 other product NDCs are listed under this name. See all Pain Relief NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Pain Relief products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Pain Reliefacetaminophen | Acetaminophen 325 mg/1 | TabletOral | Shield Pharmaceuticals Corp. | 83059-0160 | — |
| Pain Reliefmenthol spray | Menthol 76.6 mg/mL | SprayTopical | Owell Naturals Brand, LLC | 83570-003 | 83570-0003-02 |
| Pain Reliefarnica montana, belladonna, gelsemium sempervirens, gnaphalium polycephalum, magnesia phosphorica, sanguinaria canadensis, salix alba | Arnica montana whole 6 [hp_X]/1 + 6 more ingredients | TabletOral | NaturalCare | 70163-0022 | 70163-0022-01 |
| pain reliefacetaminophen | Acetaminophen 500 mg/1 | Tablet, Film coatedOral | HyVee Inc | 42507-813 | 42507-0813-78 |
| Pain Reliefmenthol | Menthol 10.5 g/100mL | SprayTopical | Trifecta Pharmaceuticals USA, LLC. | 69396-175 | 69396-0175-03 |
| Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | TabletOral | HYVEE INC | 42507-103 | 42507-0103-04 |
| Pain Reliefacetaminophen | Acetaminophen 650 mg/1 | Tablet, Extended releaseOral | HYVEE INC | 42507-303 | 42507-0303-03 |
| Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | Tablet, CoatedOral | HYVEE INC | 42507-404 | 42507-0404-09 |
| Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | Tablet, CoatedOral | HYVEE INC | 42507-592 | 42507-0592-03 |
| Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | Tablet, CoatedOral | HYVEE INC | 42507-170 | 42507-0170-0142507-0170-0242507-0170-03+1 more |
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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