NDC 70797-320

Dr Talbots Infant Mucus Cold Relief

Eupatorium Perf 12x,hepar Sulphuris Calcareum 12x,kali Bichromicum 12x,marrubium Vulgare 12x,phosphorus 30x,pulsatilla 12x,rumex Crispus 12x,sambucus Nigra 12x,calcarea Sulphurica 12x,ferrum Phosphoricum 12x

Dr Talbots Infant Mucus Cold Relief is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Talbot. The primary component is Anemone Pulsatilla; Calcium Sulfate Anhydrous; Calcium Sulfide; Eupatorium Perfoliatum Flowering Top; Ferrosoferric Phosphate; Marrubium Vulgare; Phosphorus; Potassium Chloride; Potassium Dichromate; Rumex Crispus Root; Sambucus Nigra Flowering Top.

Product ID70797-320_e8917c54-f4c3-3427-e053-2995a90adbf2
NDC70797-320
Product TypeHuman Otc Drug
Proprietary NameDr Talbots Infant Mucus Cold Relief
Generic NameEupatorium Perf 12x,hepar Sulphuris Calcareum 12x,kali Bichromicum 12x,marrubium Vulgare 12x,phosphorus 30x,pulsatilla 12x,rumex Crispus 12x,sambucus Nigra 12x,calcarea Sulphurica 12x,ferrum Phosphoricum 12x
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2022-09-12
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameTalbot
Substance NameANEMONE PULSATILLA; CALCIUM SULFATE ANHYDROUS; CALCIUM SULFIDE; EUPATORIUM PERFOLIATUM FLOWERING TOP; FERROSOFERRIC PHOSPHATE; MARRUBIUM VULGARE; PHOSPHORUS; POTASSIUM CHLORIDE; POTASSIUM DICHROMATE; RUMEX CRISPUS ROOT; SAMBUCUS NIGRA FLOWERING TOP
Active Ingredient Strength12 [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_Q]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL
Pharm ClassesBlood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 70797-320-01

1 BOTTLE in 1 CARTON (70797-320-01) > 118 mL in 1 BOTTLE
Marketing Start Date2022-09-12
NDC Exclude FlagN
Sample Package?N

Drug Details


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