Arnica
- Product NDC
- 53645-1000
- 11-digit product format
- 536451000
- Labeler code
- 53645
- Product ID
- 53645-1000_bd7a27d1-ffb1-4cbb-ae8f-cf30c92ce46a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- True Botanica, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-11-13
- Marketing end
- 0000-00-00
- Substance
- ARNICA MONTANA FLOWER
- Active strength
- 6 [hp_X]/50mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 53645-1000-0 | Arnica | 50 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 50 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53645-1000 | ARNICA LIQUID [TRUE BOTANICA, LLC] | 1 | Legacy NDC, 1 package rows | 20121121_1a5d144b-fe2d-4ff6-99fd-556c79df8678.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 53645-1000-0 | 53645100000 | 50 mL in 1 BOTTLE, WITH APPLICATOR | 50 ml | Historical |