Nivexis Dmso Multi-Relief Repair Cream
- Product NDC
- 83091-003
- 11-digit product format
- 830910003
- Labeler code
- 83091
- Product ID
- 83091-003_5ca9fed3-9dc4-9dc2-e063-6294a90a1077
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dmso Multi-Relief Repair Cream
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Anhui grass coral biotechnology Co., LTD
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-30
- Substance
- MENTHOL
- Active strength
- 2 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nivexis Dmso Multi-Relief Repair Cream
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MENTHOL | 2 g/100mL |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 83091-003-01 | 83091000301 | 118 mL in 1 BOTTLE (83091-003-01) | 118 ml | 2026-09-30 | No | No | Current |