Carbo Chamomilla
- Product NDC
- 48951-3206
- 11-digit product format
- 489513206
- Labeler code
- 48951
- Product ID
- 48951-3206_6a99d906-cf1e-7679-e053-2991aa0a1b87
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Carbo Chamomilla
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- ACTIVATED CHARCOAL; WORMWOOD; MATRICARIA RECUTITA; GENTIANA LUTEA ROOT; AVENS EXTRACT; BLACK PEPPER; GINGER; ANTIMONY TRISULFIDE; ARSENIC TRIOXIDE
- Active strength
- 2 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 48951-3206-7 | 48951320607 | 1 POWDER in 1 BOTTLE, GLASS (48951-3206-7) | 1 powder | 2009-09-01 | 0000-00-00 | No | No | Current |