BonicaEaseX Menthol Pain Relieving
- Product NDC
- 75568-043
- 11-digit product format
- 755680043
- Labeler code
- 75568
- Product ID
- 75568-043_4f1bd117-096a-4915-e063-6394a90a8a43
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, UNSPECIFIED FORM
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Planet (Anhui) Pharmaceutical Co.,Ltd
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-31
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 40 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BonicaEaseX Menthol Pain Relieving
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 40 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 415974 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75568-043-00 | BonicaEaseX Menthol Pain Relieving | 3 in 1 BOX | GEL | 3 | | 1 |
| 75568-043-00 | BonicaEaseX Menthol Pain Relieving | 118 mL in 1 TUBE | GEL | 118 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 75568-043-00 | 75568004300 | 3 TUBE in 1 BOX (75568-043-00) / 118 mL in 1 TUBE | 3 tube | 2026-03-31 | No | No | Historical |