Arnica Active Roll-On
- Product NDC
- 59262-102
- 11-digit product format
- 592620102
- Labeler code
- 59262
- Product ID
- 59262-102_60a615bb-306b-450f-944f-eb5181daa33a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica Montana
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Similasan Corporation
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2017-02-01
- Marketing end
- 0000-00-00
- Substance
- ARNICA MONTANA
- Active strength
- 1 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59262-102-42 | Arnica Active Roll-On | 74 mL in 1 APPLICATOR | LIQUID | 74 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59262-102 | ARNICA ACTIVE ROLL-ON (ARNICA MONTANA) LIQUID [SIMILASAN CORPORATION] | 1 | Legacy NDC, 1 package rows | 20170201_2ff0363f-9d37-48b3-b97e-07154e04a1de.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 59262-102-42 | 59262010242 | 74 mL in 1 APPLICATOR | 74 ml | Historical |