OxyRub Pro Pain Relief
- Product NDC
- 70015-655
- 11-digit product format
- 700150655
- Labeler code
- 70015
- Product ID
- 70015-655_d417edfb-86ce-4554-b1ce-ce126af62abb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol, Methyl Salicylate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Healthy Directions, LLC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-09-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL; METHYL SALICYLATE
- Active strength
- 25 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70015-655-04 | OxyRub Pro Pain ReliefCream, 4oz | 1 in 1 CARTON | CREAM | 1 | | 1 |
| 70015-655-04 | OxyRub Pro Pain ReliefCream, 4oz | 114 g in 1 TUBE | CREAM | 114 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70015-655 | OXYRUB PRO PAIN RELIEF CREAM, 4OZ (MENTHOL, METHYL SALICYLATE) CREAM [HEALTHY DIRECTIONS, LLC] | 1 | Legacy NDC, 2 package rows | 20170901_be26909d-afbb-4b89-a64a-fd130de223c7.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 |
|---|
| 70015-655-04 | 70015065504 | 1 TUBE in 1 CARTON (70015-655-04) > 114 g in 1 TUBE | 1 tube | 2017-09-01 | 0000-00-00 | No | No | Current |