Superior Analgesic
- Product NDC
- 58350-000
- 11-digit product format
- 583500000
- Labeler code
- 58350
- Product ID
- 58350-000_9777bbcb-7ad0-4cf6-9864-026ea343b125
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Superior Analgesic
- Dosage form
- LINIMENT
- Route
- TRANSDERMAL
- Labeler
- Superior Trading Company
- Application
- part346
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2009-12-28
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 4 mg/100mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 58350-000-00 | Superior Analgesic | 100 mL in 1 BOTTLE | LINIMENT | 100 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58350-000 | SUPERIOR ANALGESIC LINIMENT [SUPERIOR TRADING COMPANY] | 1 | Legacy NDC, 1 package rows | 20091229_9777bbcb-7ad0-4cf6-9864-026ea343b125.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 58350-000-00 | 58350000000 | 100 mL in 1 BOTTLE | 100 ml | Historical |