70797-320 NDC - 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)

Drug Information

  • Product NDC: 70797-320
  • Proprietary Name: Dr Talbots Infant Mucus Cold Relief
  • Non Proprietary Name: 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
  • Active Ingredient(s): 12 [hp_X]/118mL ANEMONE PULSATILLA; 12 [hp_X]/118mL CALCIUM SULFATE ANHYDROUS; 12 [hp_X]/118mL CALCIUM SULFIDE; 12 [hp_X]/118mL EUPATORIUM PERFOLIATUM FLOWERING TOP; 12 [hp_X]/118mL FERROSOFERRIC PHOSPHATE; 12 [hp_Q]/118mL MARRUBIUM VULGARE; 30 [hp_X]/118mL PHOSPHORUS; 6 [hp_X]/118mL POTASSIUM CHLORIDE; 12 [hp_X]/118mL POTASSIUM DICHROMATE; 12 [hp_X]/118mL RUMEX CRISPUS ROOT; 12 [hp_X]/118mL SAMBUCUS NIGRA FLOWERING TOP
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Blood 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]

Labeler Information

Field Name Field Value
Labeler Name: Talbot�s Pharmaceuticals Family Products, LLC.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/12/2022

Package Information

No. Package Code Package Description Billing Unit
170797-320-011 BOTTLE in 1 CARTON (70797-320-01) / 118 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC70797-320The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEDr Talbots Infant Mucus Cold ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY 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 12XThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE9/12/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMETalbot�s Pharmaceuticals Family Products, LLC.Name of Company corresponding to the labeler code segment of the Product NDC.
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 TOPAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH12; 12; 12; 12; 12; 12; 30; 6; 12; 12; 12 
ACTIVE INGRED UNIT[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] 

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 3/27/2026

Previous Code
Next Code