Agaricus Albus 30X
- Product NDC
- 53645-1621
- 11-digit product format
- 536451621
- Labeler code
- 53645
- Product ID
- 53645-1621_3bb3a128-253f-5290-e063-6394a90a1797
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Agaricus Albus 30X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- True Botanica, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-09-29
- Substance
- AGARICUS BISPORUS WHOLE
- Active strength
- 30 [hp_X]/30mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings
Warnings: Consult your health care provider if symptoms persist more than 5 days or worsen.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Agaricus Albus 30X
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AGARICUS BISPORUS WHOLE | 30 [hp_X]/30mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | B0FRQ940N7 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53645-1621-6 | Agaricus Albus 30X | 30 mL in 1 BOTTLE | LIQUID | 30 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 53645-1621-6 | 53645162106 | 30 mL in 1 BOTTLE (53645-1621-6) | 30 ml | 2025-09-29 | No | No | Current |