BM Crataegus Oxy
- Product NDC
- 85816-5123
- Requested package NDC
- 85816-5123-1
- 11-digit product format
- 858165123
- Labeler code
- 85816
- Product ID
- 85816-5123_5ec00272-8bb4-881e-e063-6394a90a162f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Crataegus Oxy
- Dosage form
- TINCTURE
- Route
- ORAL
- Labeler
- BM Private Limited
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-01-01
- Substance
- CRATAEGUS FRUIT
- Active strength
- 1 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BM Crataegus Oxy
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CRATAEGUS FRUIT | 1 [hp_X]/mL |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85816-5123-1 | BM 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 |
|---|
| 85816-5123-1 | 85816512301 | 30 mL in 1 BOTTLE, GLASS (85816-5123-1) | 30 ml | 2015-01-01 | No | No | Current |