Joint Analgesic Plaster
- Product NDC
- 42217-205
- 11-digit product format
- 422170205
- Labeler code
- 42217
- Product ID
- 42217-205_499a0613-2d47-46ad-afae-12b38dbde14b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Camphor
- Dosage form
- PLASTER
- Route
- TRANSDERMAL
- Labeler
- Henan Lingrui Pharmaceutical Co Ltd
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-06-02
- Marketing end
- 0000-00-00
- Substance
- CAMPHOR (SYNTHETIC)
- Active strength
- 3 g/100g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42217-205-10 | Joint Analgesic Plaster | 10 in 1 BOX | PLASTER | 10 | | 3105 |
| 42217-205-10 | Joint Analgesic Plaster | 1 g in 1 PATCH | PLASTER | 1 | | 3105 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42217-205 | JOINT ANALGESIC PLASTER (CAMPHOR) PLASTER [HENAN LINGRUI PHARMACEUTICAL CO LTD] | 3105 | Legacy NDC, 2 package rows | 20150313_ba27c3d6-4826-4a78-b166-d1b722e7095c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 42217-205-10 | 42217020510 | 10 in 1 BOX | Historical |