Arnica Plus
- Product NDC
- 70163-0203
- 11-digit product format
- 701630203
- Labeler code
- 70163
- Product ID
- 70163-0203_16eac908-76bc-4c55-a1e7-845415b5b45c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica Montana, Hamamelis Virginiana, Rhus Tox
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- NaturalCare
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2026-09-11
- Substance
- ARNICA MONTANA WHOLE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; TOXICODENDRON PUBESCENS LEAF
- Active strength
- 6; 6; 6 [hp_X]/g; [hp_X]/g; [hp_X]/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 Plus
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARNICA MONTANA WHOLE | 6 [hp_X]/g |
| HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK | 6 [hp_X]/g |
| TOXICODENDRON PUBESCENS LEAF | 6 [hp_X]/g |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70163-0203-2 | 70163020302 | 1 BOTTLE, PUMP in 1 CARTON (70163-0203-2) / 113.4 g in 1 BOTTLE, PUMP (70163-0203-1) | 2026-09-11 | No | No | Current |