Crataegus Oxy
- Product NDC
- 82969-5123
- 11-digit product format
- 829695123
- Labeler code
- 82969
- Product ID
- 82969-5123_36d4496c-297f-520d-e063-6294a90ab458
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Crataegus Oxyacantha (HPUS)
- Dosage form
- TINCTURE
- Route
- ORAL
- Labeler
- Bestmade Natural Products
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-06-01
- Substance
- CRATAEGUS FRUIT
- Active strength
- 1 [hp_M]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Crataegus Oxy
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CRATAEGUS FRUIT | 1 [hp_M]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Q21UUL2105 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82969-5123-1 | Crataegus Oxy | 30 mL in 1 BOTTLE, GLASS | TINCTURE | 30 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82969-5123-1 | 82969512301 | 30 mL in 1 BOTTLE, GLASS (82969-5123-1) | 30 ml | 2025-06-01 | No | No | Current |