Dakota Muscle Relief Roll-On
- Product NDC
- 71680-002
- 11-digit product format
- 716800002
- Labeler code
- 71680
- Product ID
- 71680-002_143397ce-e7b9-4eb2-8fa2-6b2ce8f088af
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, UNSPECIFIED FORM
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- LaShe Naturals, LLC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2011-11-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 60 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71680-002 | DAKOTA MUSCLE RELIEF ROLL-ON (MENTHOL, UNSPECIFIED FORM) SOLUTION [LASHE NATURALS, LLC] | 3 | Legacy NDC | 20211212_880d39d5-63ba-42c2-996a-78b835550524.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71680-002-03 | 71680000203 | 90 mL in 1 BOTTLE, WITH APPLICATOR (71680-002-03) | 90 ml | 2017-09-19 | 0000-00-00 | No | No | Current |