- Product NDC
- 57955-5152
- 11-digit product format
- 579555152
- Labeler code
- 57955
- Product ID
- 57955-5152_6082dd4c-f6a3-421c-bc8c-f1133691939b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Abelmoschus, Aconitum napellus, Argentum nitricum, Arsenicum album, Calcarea carbonica, Cinchona officinalis, Cocculus indicus, Gelsemium sempervirens, Kali arsenicosum, Lilium tigrinum, Lycopodium clavatum, Phosphorus, Pulsatilla and Stramonium
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-10-11
- Marketing end
- 0000-00-00
- Substance
- ABELMOSCHUS MOSCHATUS SEED; ACONITUM NAPELLUS; SILVER NITRATE; ARSENIC TRIOXIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CINCHONA OFFICINALIS BARK; ANAMIRTA COCCULUS SEED; GELSEMIUM SEMPERVIRENS ROOT; POTASSIUM ARSENITE ANHYDROUS; LILIUM LANCIFOLIUM WHOLE FLOWERING; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; PULSATILLA VULGARIS; DATURA STRAMONIUM
- 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
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record