FEMININE PAIN RELIEF
- Product NDC
- 71391-130
- 11-digit product format
- 713910130
- Labeler code
- 71391
- Product ID
- 71391-130_94875a1d-da37-4c18-a673-25fa696edcf1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, UNSPECIFIED FORM
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- Unexo Life Sciences, Private Limited
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-01-19
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FEMININE PAIN RELIEF
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71391-130-05 | FEMININE PAIN RELIEF | 5 in 1 POUCH | PATCH | 5 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71391-130 | FEMININE PAIN RELIEF (MENTHOL, UNSPECIFIED FORM) PATCH [UNEXO LIFE SCIENCES, PRIVATE LIMITED] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250115_30d6241f-9fca-4a1a-a509-1274007debb3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71391-130-05 | 71391013005 | 5 PATCH in 1 POUCH (71391-130-05) | 5 patch | 2019-01-19 | 0000-00-00 | No | No | Current |