SUNMED MOTION
- Product NDC
- 73240-902
- 11-digit product format
- 732400902
- Labeler code
- 73240
- Product ID
- 73240-902_ab6d01ad-61f7-438b-ae5b-57ab51156bb6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Sunflora Inc
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-08-22
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE
- Active strength
- 4 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 73240-902-11 | SUNMED MOTION | 1 in 1 BOX | LIQUID | 1 | | 1 |
| 73240-902-11 | SUNMED MOTION | 74 mL in 1 BOTTLE | LIQUID | 74 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73240-902 | SUNMED MOTION (LIDOCAINE) LIQUID [SUNFLORA INC] | 1 | Legacy NDC, 2 package rows | 20190828_1ef36715-2b45-441e-9f61-d99b8d553d11.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73240-902-11 | 73240090211 | 1 BOTTLE in 1 BOX (73240-902-11) > 74 mL in 1 BOTTLE | 1 bottle | 2019-08-22 | 0000-00-00 | No | No | Current |