AcuPlus Advanced Therapy for Pain and Recovery
- Product NDC
- 72037-136
- 11-digit product format
- 720370136
- Labeler code
- 72037
- Product ID
- 72037-136_0974c990-eb0f-73ff-e063-6294a90af414
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- INNOVATIONS FOR WELLNESS, LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-05-01
- Substance
- MENTHOL
- Active strength
- 35 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
- AcuPlus Advanced Therapy for Pain and Recovery
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 35 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 1089766 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72037-136-03 | AcuPlus Advanced Therapy for Pain and Recovery | 89 mL in 1 TUBE | SOLUTION | 89 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72037-136 | ACUPLUS ADVANCED THERAPY FOR PAIN AND RECOVERY (MENTHOL) SOLUTION [INNOVATIONS FOR WELLNESS, LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231106_840cfd15-4ea1-49bf-8c4f-86c12461d860.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 |
|---|
| 72037-136-03 | 72037013603 | 89 mL in 1 TUBE (72037-136-03) | 89 ml | 2019-05-01 | 0000-00-00 | No | No | Current |