Rheumatism
- Product NDC
- 43742-0001
- 11-digit product format
- 437420001
- Labeler code
- 43742
- Product ID
- 43742-0001_39c22b27-2f78-4d0e-9394-36543c6c4a31
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoicum acidum, Pulsatilla, Rhododendron chrysanthum, Spiraea ulmaria, Aconitum napellus, Dulcamara, Euphorbium officinarum, Ledum palustre, Asclepias tuberosa, Lithium benzoicum,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-04-05
- Marketing end
- 2020-09-25
- Substance
- BENZOIC ACID; PULSATILLA VULGARIS; RHODODENDRON AUREUM LEAF; FILIPENDULA ULMARIA ROOT; ACONITUM NAPELLUS; SOLANUM DULCAMARA FLOWER; EUPHORBIA RESINIFERA RESIN; LEDUM PALUSTRE TWIG; ASCLEPIAS TUBEROSA ROOT; LITHIUM BENZOATE
- 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
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record