URIFLEX Fast Acting Analgesic Pain Relief
- Product NDC
- 73168-004
- 11-digit product format
- 731680004
- Labeler code
- 73168
- Product ID
- 73168-004_09751fc7-6657-c196-e063-6294a90a4a57
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Rejuvica LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-05-20
- Substance
- MENTHOL
- Active strength
- 45 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- URIFLEX Fast Acting Analgesic Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 45 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 2171392 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73168-004-00 | URIFLEX Fast Acting Analgesic Pain Relief | 118 mL in 1 JAR | CREAM | 118 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73168-004 | URIFLEX FAST ACTING ANALGESIC PAIN RELIEF (MENTHOL) CREAM [REJUVICA LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231106_fb78f705-b838-461d-b42c-8c98d3ca5d09.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 |
|---|
| 73168-004-00 | 73168000400 | 118 mL in 1 JAR (73168-004-00) | 118 ml | 2019-05-20 | 0000-00-00 | No | No | Current |