FEMININE PAIN RELIEF
- Product NDC
- 84253-001
- 11-digit product format
- 842530001
- Labeler code
- 84253
- Product ID
- 84253-001_473fdd7c-e667-7f3c-e063-6294a90a5561
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, UNSPECIFIED FORM
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- BeYou Together Ltd
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-07-14
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 10 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 | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 2621715 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84253-001-01 | FEMININE PAIN RELIEF | 5 in 1 POUCH | PATCH | 5 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84253-001-01 | 84253000101 | 5 PATCH in 1 POUCH (84253-001-01) | 5 patch | 2025-07-14 | No | No | Current |