Aconitum Bryonia Adult
- Product NDC
- 48951-1351
- 11-digit product format
- 489511351
- Labeler code
- 48951
- Product ID
- 48951-1351_c9607d3a-af8c-4ec3-e053-2a95a90a6875
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum Bryonia Adult
- Dosage form
- SUPPOSITORY
- Route
- RECTAL
- Labeler
- Uriel Pharmacy
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- ATROPA BELLADONNA; EUCALYPTUS GUM; SILVER; ECHINACEA, UNSPECIFIED; CINCHONA OFFICINALIS BARK; EUPATORIUM PERFOLIATUM FLOWERING TOP; ACONITUM NAPELLUS; BRYONIA ALBA ROOT
- Active strength
- 3 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1351-1 | 48951135101 | 10 BLISTER PACK in 1 BAG (48951-1351-1) > 1 g in 1 BLISTER PACK | 10 blister pack | 2009-09-01 | 0000-00-00 | No | No | Current |