ARNICA BRUISE
- Product NDC
- 88028-003
- 11-digit product format
- 880280003
- Labeler code
- 88028
- Product ID
- 88028-003_5f47f7cc-d5f5-5037-e063-6394a90a9d2a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica montana
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Shenzhen Fanyi Era Technology Co., Ltd
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2026-11-02
- Substance
- ARNICA MONTANA
- Active strength
- 70 mg/g
- 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
- ARNICA BRUISE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARNICA MONTANA | 70 mg/g |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 88028-003-01 | 88028000301 | 1 BOTTLE in 1 BOX (88028-003-01) / 113 g in 1 BOTTLE | 1 bottle | 2026-11-02 | No | No | Current |