IQVPPW ARNICA BRUISE Cream
- Product NDC
- 87786-069
- 11-digit product format
- 877860069
- Labeler code
- 87786
- Product ID
- 87786-069_5c37d1e9-d9f9-ac64-e063-6294a90aa886
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica Montana 1X HPUS 7% ARNICA BRUISE Cream
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Wenzhou Yuyuan Pharmaceutical Co., Ltd.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-17
- Substance
- ARNICA MONTANA
- Active strength
- 7 g/100g
- 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
- IQVPPW ARNICA BRUISE Cream
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ARNICA MONTANA | 7 g/100g |
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 |
|---|---|---|---|---|---|---|---|
| 87786-069-01 | 87786006901 | 120 g in 1 BOTTLE (87786-069-01) | 120 g | 2026-09-17 | No | No | Current |