- Product NDC
- 68703-116
- 11-digit product format
- 687030116
- Labeler code
- 68703
- Product ID
- 68703-116_7ef8d2be-6f2a-440c-8ca0-7522d9c86ef9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alumen, Benzoicum acidum, Cadmium sulphuricum, Chelidonium majus, Colchicum autumnale, Dulcamara, Hypothalamus, Manganum aceticum, Mercurius solubilis, Natrum muriaticum, Nitricum acidum, Phosphorus, Ranunculus bulbosus, Rhododendron chrysanthum, Thyroidinum
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Native Remedies, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-07-24
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM ALUM; BENZOIC ACID; CADMIUM SULFATE; CHELIDONIUM MAJUS; COLCHICUM AUTUMNALE BULB; SOLANUM DULCAMARA TOP; BOS TAURUS HYPOTHALAMUS; MANGANESE ACETATE TETRAHYDRATE; MERCURIUS SOLUBILIS; SODIUM CHLORIDE; NITRIC ACID; PHOSPHORUS; RANUNCULUS BULBOSUS; RHODODENDRON AUREUM LEAF; THYROID, UNSPECIFIED
- Active strength
- 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record