Inflammation
- Product NDC
- 43742-0472
- 11-digit product format
- 437420472
- Labeler code
- 43742
- Product ID
- 43742-0472_0aaa7890-cfa7-4281-8655-a5c65dc83a9b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Eupatorium Perfoliatum, Arnica Montana, Benzoicum Acidum, Echinacea (Angustifolia), Mercurialis Perennis, Apis Mellifica, Baptisia Tinctoria, Bryonia (Alba), Colchicum Autumnale, Dulcamara, Eucalyptus Globulus, Solanum Nigrum, Rhus Tox
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-03-21
- Marketing end
- 2021-02-11
- Substance
- EUPATORIUM PERFOLIATUM FLOWERING TOP; ARNICA MONTANA; BENZOIC ACID; ECHINACEA ANGUSTIFOLIA; MERCURIALIS PERENNIS; APIS MELLIFERA; BAPTISIA TINCTORIA ROOT; BRYONIA ALBA ROOT; COLCHICUM AUTUMNALE BULB; SOLANUM DULCAMARA TOP; EUCALYPTUS GLOBULUS LEAF; SOLANUM NIGRUM WHOLE; TOXICODENDRON PUBESCENS LEAF
- Active strength
- 2 [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