Swift River Pain Relief
- Product NDC
- 73596-200
- 11-digit product format
- 735960200
- Labeler code
- 73596
- Product ID
- 73596-200_9400c94f-014f-4924-834d-ec29342af070
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE and MENTHOL, UNSPECIFIED FORM
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Philia Group LLC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-17
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE; MENTHOL, UNSPECIFIED FORM
- Active strength
- 4000 mg/113g; mg/113g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 73596-200-01 | Swift River Pain Relief | 113 g in 1 BOTTLE | CREAM | 113 | | 1 |
| 73596-200-01 | Swift River Pain Relief | 1 in 1 BOX | CREAM | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73596-200 | SWIFT RIVER PAIN RELIEF (LIDOCAINE HYDROCHLORIDE AND MENTHOL, UNSPECIFIED FORM) CREAM [PHILIA GROUP LLC] | 1 | Legacy NDC, 2 package rows | 20200817_28cab17e-1f7d-4948-aea7-138e1f27436c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73596-200-01 | 73596020001 | 1 BOTTLE in 1 BOX (73596-200-01) > 113 g in 1 BOTTLE | 1 bottle | 2020-08-17 | 0000-00-00 | No | No | Current |