Asthmaforce
- Product NDC
- 43857-0032
- 11-digit product format
- 438570032
- Labeler code
- 43857
- Product ID
- 43857-0032_6d0bb145-0c40-47b6-9bb9-adb5b6859dc1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica montana, Asclepias tuberosa, Eriodictyon californicum, Eucalyptus globulus, Lobelia inflata, Plantago major, Trifolium pratense, Arsenicum album, Belladonna, Bryonia, Carbo vegetabilis, Grindelia, Kali carbonicum, Natrum sulphuricum, Pulsatilla,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-06-01
- Marketing end
- 2024-04-01
- Substance
- ARNICA MONTANA; ASCLEPIAS TUBEROSA ROOT; ERIODICTYON CALIFORNICUM LEAF; EUCALYPTUS GLOBULUS LEAF; LOBELIA INFLATA; PLANTAGO MAJOR; TRIFOLIUM PRATENSE FLOWER; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BRYONIA ALBA ROOT; ACTIVATED CHARCOAL; GRINDELIA HIRSUTULA FLOWERING TOP; POTASSIUM CARBONATE; SODIUM SULFATE; PULSATILLA VULGARIS
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 43857-0032-1 | 43857003201 | 30 mL in 1 BOTTLE, DROPPER (43857-0032-1) | 30 ml | 2016-06-22 | 2024-04-01 | No | No | Current |