NDC 53645-1201
Anacardium
Anacardium
Anacardium is a Oral Globule in the Human Otc Drug category. It is labeled and distributed by True Botanica, Llc. The primary component is Sulfur.
| Product ID | 53645-1201_6198f81e-c783-9f38-e053-2a91aa0a52c3 |
| NDC | 53645-1201 |
| Product Type | Human Otc Drug |
| Proprietary Name | Anacardium |
| Generic Name | Anacardium |
| Dosage Form | Globule |
| Route of Administration | ORAL |
| Marketing Start Date | 2014-02-03 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | True Botanica, LLC |
| Substance Name | SULFUR |
| Active Ingredient Strength | 30 [hp_X]/23g |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
Packaging
NDC 53645-1201-2
23 g in 1 BOTTLE (53645-1201-2)
| Marketing Start Date | 2014-02-03 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 53645-1201-2 [53645120102]
Anacardium GLOBULE
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-02-03 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| SULFUR | 30 [hp_X]/23g |
OpenFDA Data
| SPL SET ID: | 6198f81e-c782-9f38-e053-2a91aa0a52c3 |
| Manufacturer | |
| UNII |
NDC Crossover Matching brand name "Anacardium" or generic name "Anacardium"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 53645-1201 | Anacardium | Anacardium |
| 53645-1490 | Anacardium | Anacardium |
| 53645-1491 | Anacardium | Anacardium |
| 53645-1560 | Anacardium | Anacardium |
| 53645-1630 | Anacardium | Anacardium |
| 53645-1870 | Anacardium | Anacardium |
Trademark Results [Anacardium]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ANACARDIUM 76387251 2909477 Dead/Cancelled |
Anacardium LLC 2002-03-26 |
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